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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66099

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

Open FDA event record

Event summary

Timeline bucket
August 23, 2013
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
JCB Labs 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

5 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 5

Acetylcysteine 20% Solution, Preservative Free, 4 mL Sterile Single Dose Vial, Not for Injection, Sterile Solution For Office Use Only, JCB Laboratories, Wichita, KS.

D-1043-2013
Recall number
D-1043-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
JCB Labs LLC
Quantity
903 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination
Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

Lot # 130627@5, Exp 08/26/2013

Distribution pattern

Nationwide and Guam

drug · product 2 of 5

Sodium Thiosulfate 25%, 250 mg/mL (12.5 g/50mL), PF Sterile Solution for Injection, 50 mL Single Dose Vial, For Office Use Only, JCB Laboratories, Wichita, KS.

D-1044-2013
Recall number
D-1044-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
JCB Labs LLC
Quantity
1056 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination
Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

Lot #: 130701@9, Exp 12/28/2013; 130709@6, Exp 01/05/2014; 130717@2, Exp 01/13/2014

Distribution pattern

Nationwide and Guam

drug · product 3 of 5

Sodium Citrate 4% containing Gentamicin 320 mcg/mL, Solution for Injection, 30 mL Multi Dose Vial, Sterile Solution For Office Use Only, JCB Laboratories, Wichita, KS.

D-1045-2013
Recall number
D-1045-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
JCB Labs LLC
Quantity
397 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination
Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

Lot # 130620@2, Exp 12/17/2013

Distribution pattern

Nationwide and Guam

drug · product 4 of 5

Sodium Citrate 4% Solution for Injection, 30 mL Multi Dose Vial, Sterile Solution for Office Use Only, JCB Laboratories, Wichita, KS.

D-1046-2013
Recall number
D-1046-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
JCB Labs LLC
Quantity
677 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination
Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

Lot # 130710@4, Exp. 01/06/2014

Distribution pattern

Nationwide and Guam

drug · product 5 of 5

Epinephrine 1:1,000 (1mg/mL) Sterile Solution for injection, Preservative Free/Sulfite Free, 1-mL Single-Use Syringe, Sterile Solution For Office Use Only, JCB Laboratories, Wichita, KS.

D-1047-2013
Recall number
D-1047-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
JCB Labs LLC
Quantity
1243 Syringes

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial contamination
Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

Lot # 130806@2, Expiry 09/20/2013.

Distribution pattern

Nationwide and Guam

Field note

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