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CriticalClass ITerminated

FDA Drug recall · Reported August 14, 2013

Piperacillin and Tazobactam for Injection, USP, 40.5 grams per Pharmacy Bulk Package vial, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd., Irungattukottai - 602 105, India; Mfg. for: Apotex Corp., Weston, FL 33326, NDC 60505-0773-0

Crystallization: Potential to exhibit precipitation/crystallization in IV bag or IV line upon reconstitution.

Recall #
D-835-2013
Affected scope
52,398 vials
Initiated
May 10, 2013
Verify with FDA Drug →
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Apotex Corp. recalled Piperacillin and Tazobactam for Injection, USP, 40.5 grams per Pharmacy Bulk Package vial… - a critical-severity action.

Piperacillin and Tazobactam for Injection, USP, 40.5 grams per Pharmacy Bulk Package vial… was recalled by Apotex Corp. in August 14, 2013. Reason: Crystallization: Potential to exhibit precipitation/crystallization in IV bag or IV line upon reconstitution.. Check the official notice for the remedy. Verify recall #D-835-2013 with the FDA Drug before acting.

The recall

Apotex Corp. issued this critical-severity FDA Drug recall-Crystallization: Potential to exhibit precipitation/crystallization in IV bag or IV line upon reconstitution..

Critical
severity level
Class I
classification
August 14, 2013
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-835-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,472 drugs & medications recalls on record

05001,0001,5002,000 2006201220152018202120242026 448
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Piperacillin and Tazobactam for Injection, USP, 40.5 grams per Pharmacy Bulk Package vial, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd., Irungattukottai - 602 105, India; Mfg. for: Apotex Corp., Weston, FL 33326, NDC 60505-0773-0

Reason for recall

Crystallization: Potential to exhibit precipitation/crystallization in IV bag or IV line upon reconstitution.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number D-835-2013
Date reported August 14, 2013
Date initiated May 10, 2013
Recalling firm Apotex Corp.
Firm location Weston, FL
Affected scope 52,398 vials
Distribution Nationwide

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-835-2013) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Piperacillin and Tazobactam for Injection, USP, 40.5 grams per Pharmacy Bulk Package vial, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd., Irungattukottai - 602 105, India; Mfg. for: Apotex Corp., Weston, FL 33326, NDC 60505-0773-0. Recalled by Apotex Corp.. Units affected: 52,398 vials.
Why was this product recalled?
Crystallization: Potential to exhibit precipitation/crystallization in IV bag or IV line upon reconstitution.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 14, 2013. Severity: Critical. Recall number: D-835-2013.
Where was the recalled product distributed?
Distribution: Nationwide.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

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This recall: FDA Drug, reported August 14, 2013. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026