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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77960

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

Open FDA event record

Event summary

Timeline bucket
August 16, 2017
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Pharmatech LLC

Dossier provenance

Source snapshots represented here

  • openFDA Drug 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

Complete imported group

Every recalled product in this event

4 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.

drug · product 1 of 4

Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85, Manufactured by PharmaTech LLC, Davie, FL

D-0224-2018
Recall number
D-0224-2018
Initiated
August 16, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pharmatech LLC
Quantity
Unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination

Code information

All lots remaining within expiry.

Distribution pattern

MI

drug · product 2 of 4

Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1001-85, Manufactured by PharmaTech LLC, Davie, FL

D-0225-2018
Recall number
D-0225-2018
Initiated
August 16, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pharmatech LLC
Quantity
Unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination

Code information

All lots remaining within expiry.

Distribution pattern

MI

drug · product 3 of 4

Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59 ; ALSO LABELED AS Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09; Manufactured by PharmaTech LLC, Davie, FL

D-0226-2018
Recall number
D-0226-2018
Initiated
August 16, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pharmatech LLC
Quantity
Unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination

Code information

All lots remaining within expiry.

Distribution pattern

MI

drug · product 4 of 4

Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47, Manufactured by PharmaTech LLC, Davie FL

D-0227-2018
Recall number
D-0227-2018
Initiated
August 16, 2017
Classification
Class II
Status
Terminated
Recalling firm
Pharmatech LLC
Quantity
Unknown

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination

Code information

All lots remaining within expiry.

Distribution pattern

MI

Field note

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