Exact FDA event identifier

Event 75272

23 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: August 08, 2016
Product types: Food
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Pharmatech LLC

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

23 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 23

Virtrate-2, Sodium Citrate-Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

F-0254-2017

Recall number: F-0254-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 34,612 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 69543-367-16; Lot No. 28601502, Exp. Date 11/2017; Lot No. 28601601, Exp. Date 01/2018; Lot No. 28601602, Exp. Date 03/2018; Lot No. 28601603, Exp. Date 06/2018; Lot No. 28601604, Exp. Date 06/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 2 of 23

Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

F-0255-2017

Recall number: F-0255-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 8,232 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 69543-262-16; Lot No. 28891502, Exp. Date 12/2017; Lot No. 28891503, Exp. Date 12/2017.

Distribution pattern

FL, MI, MS, and OH.

food · product 3 of 23

Calcionate Syrup, Calcium Glubionate Syrup, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement.

F-0256-2017

Recall number: F-0256-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 6,048 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005362770851, Exp. Date 06/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 4 of 23

D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0257-2017

Recall number: F-0257-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 229,464 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005368400806; Lot No. 20691509, Exp. Date11/2017; Lot No. 20691601, Exp. Date 01/2018; Lot No. 20691602, Exp. Date 02/2018; Lot No. 20691604, Exp. Date 05/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 5 of 23

Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.

F-0258-2017

Recall number: F-0258-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 129,268 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005362790590; Lot No. 20471516, 20471517, 20471518, 20471519, & 20471520, Exp. Date 11/2017; Lot No. 20471521, Exp. Date 12/2017; Lot No. 20471601, Exp. Date 01/2018; Lot No. 20471608, Exp. Date 04/2018; Lot No. 20471610 & 20471613, Exp. Date 05/2018; Lot No. 20471614, Exp. Date 06/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 6 of 23

Ferrous Sulfate Liquid, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement.

F-0259-2017

Recall number: F-0259-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 75,972 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005360650858; Lot No. 22461511 & 22461512, Exp. Date 10/2017; Lot No. 22461513 & 22461514, Exp. Date 11/2017; Lot No. 22461515 & 22461516, Exp. Date 12/2017; Lot No. 22461601 & 22461602, Exp. Date 02/2018; Lot No. 22461603 & 22461604, Exp. Date 04/2018; Lot No. 22461605 & 22461606, Exp. Date 05/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 7 of 23

Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0260-2017

Recall number: F-0260-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 99,024 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005360710804; Lot No. 20901507, Exp. Date 07/2017; Lot No. 20901507, Exp. Date 11/2017; Lot No. 20901603, Exp. Date 05/2018

Distribution pattern

FL, MI, MS, and OH.

food · product 8 of 23

Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0261-2017

Recall number: F-0261-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 201,784 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005360710801; Lot No. 21021510, Exp. Date 07/2017; Lot No. 21021601, Exp. Date 01/2018; Lot No. 21021602, Exp. Date 02/2018; Lot No. 21021604, Exp. Date 05/2016.

Distribution pattern

FL, MI, MS, and OH.

food · product 9 of 23

Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0262-2017

Recall number: F-0262-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 188,640 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005368450801; Lot No. 20701511, Exp. Date 09/2018; Lot No. 20701514, Exp. Date 12/2017; Lot No. 20701605, Exp. Date 05/2018; Lot No. 20701606, Exp. Date 06/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 10 of 23

Tri-Vitamin, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0263-2017

Recall number: F-0263-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 105,456 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005368501800; Lot No. 20731506, Exp. Date 08/2017; Lot No. 20731603, Exp. Date 02/2018; Lot No. 20731604, Exp. Date 06/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 11 of 23

Liquid Vitamin C, 4 oz./118 mL, OTC Non-Sterile. Dietary supplement.

F-0264-2017

Recall number: F-0264-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 48,024 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 005360160975; Lot No. 20331510 & 20331511, Exp. Date 12/2017; Lot No. 20331601 & 20331602, Exp. Date 03/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 12 of 23

CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.

F-0265-2017

Recall number: F-0265-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 110,136 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 0904-5023-09; Lot No. 20471602, Exp. Date 01/2018; Lot No. 20471603 & 20471604, Exp. Date 02/2018; Lot No. 20471605 & 20171606, Exp. Date 03/2018; Lot No. 20471607, Exp. Date 04/2018; Lot No. 20471609, 20471611& 20471612, Exp. Date 05/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 13 of 23

Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0266-2017

Recall number: F-0266-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 42,984 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 0904-5099-50; Lot No. 20701509 & 20701511, Exp. Date 09/2017; Lot No. 20701513, Exp. Date 12/2017; Lot No. 20701601, Exp. Date 02/2018; Lot No. 20701602 & 20701603, Exp. Date 04/2018; Lot No. 20701606, Exp. Date 06/2016.

Distribution pattern

FL, MI, MS, and OH.

food · product 14 of 23

Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0267-2017

Recall number: F-0267-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 47,525 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 0904-5100-50; Lot No. 21021510, Exp. Date 07/2017; Lot No. 21021601, Exp. Date 01/2018; Lot No. 21021602, Exp. Date 02/2016; Lot No. 21021603, Exp. Date 04/2018; Lot No. 21021604, Exp. Date 05/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 15 of 23

D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0268-2017

Recall number: F-0268-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 90,504 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 0904-6273-50; Lot No. 20691509, Exp. Date 11/2017; Lot No. 20691510, Exp. Date 12/2017; Lot No. 206916603, Exp. Date 03/2018; Lot No. 20691605, Exp. Date 04/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 16 of 23

Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0269-2017

Recall number: F-0269-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 31,224 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 0904-6060-50; Lot No. 20901509 & 20901510, Exp. Date 11/2017; Lot No. 20901601, Exp. Date 02/2018; Lot No. 20901602, Exp. Date 03/2018; Lot No. 20901603, Exp. Date 05/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 17 of 23

Tri-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0270-2017

Recall number: F-0270-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 23,736 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 0904-6274-50; Lot No. 20731506, Exp. Date 08/20107; Lot No. 20731507, Exp. Date 11/2017; Lot No. 20731604 & 20731605, Exp. Date 06/2018.

Distribution pattern

FL, MI, MS, and OH.

food · product 18 of 23

Pedia Tri-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0271-2017

Recall number: F-0271-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 8,712 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 76518-020-50, Lot No. 20731506, Exp. Date 08/2017; Lot No. 20731508, Exp. Date 11/2017.

Distribution pattern

FL, MI, MS, and OH.

food · product 19 of 23

Pedia Tri-Vite Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0272-2017

Recall number: F-0272-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 6,024 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 76518-040-50, Lot No. 21021511, Exp. Date 11/2017.

Distribution pattern

FL, MI, MS, and OH.

food · product 20 of 23

Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0273-2017

Recall number: F-0273-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 6,600 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 76518-030-50; Lot No. 20701512, Exp. Date 11/2017.

Distribution pattern

FL, MI, MS, and OH.

food · product 21 of 23

Pedia D-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0274-2017

Recall number: F-0274-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 5,040 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

NDC No. 76518-050-50; Lot No. 20691509, Exp. Date 11/2017

Distribution pattern

FL, MI, MS, and OH.

food · product 22 of 23

Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.

F-0275-2017

Recall number: F-0275-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 62,228 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

Lot No. 30161601, Exp. Date 01/2018; Lot No. 30161602 & 30161603.

Distribution pattern

FL, MI, MS, and OH.

food · product 23 of 23

CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.

F-0276-2017

Recall number: F-0276-2017
Initiated: August 08, 2016
Classification: Class II
Status: Terminated
Recalling firm: Pharmatech LLC
Quantity: 1,990 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Code information

UPC No. 632687615989; Lot No. 30661601, Exp. Date 05/2018.

Distribution pattern

FL, MI, MS, and OH.