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CriticalClass ITerminated

FDA Drug recall · Reported July 18, 2018

Piperacillin and Tazobactam for Injection USP 3.375 grams per vial, Single-Dose Vial, Rx Only. Manufactured for: Auromedics Pharma LLC 6 Wheeling Road Dayton NJ 08810, Made in India. NDC 55150-120-30

Presence of Particulate Matter: identified as glass and silicone material

Recall #
D-1030-2018
Affected scope
73620 single-dose vials
Initiated
July 2, 2018
Verify with FDA Drug →
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AuroMedics Pharma LLC recalled Piperacillin and Tazobactam for Injection USP 3.375 grams per vial, Single-Dose Vial, Rx … - a critical-severity action.

Piperacillin and Tazobactam for Injection USP 3.375 grams per vial, Single-Dose Vial, Rx … was recalled by AuroMedics Pharma LLC in July 18, 2018. Reason: Presence of Particulate Matter: identified as glass and silicone material. Check the official notice for the remedy. Verify recall #D-1030-2018 with the FDA Drug before acting.

The recall

AuroMedics Pharma LLC issued this critical-severity FDA Drug recall-Presence of Particulate Matter: identified as glass and silicone material.

Critical
severity level
Class I
classification
July 18, 2018
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-1030-2018 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 3.375 grams per vial, Single-Dose Vial, Rx Only. Manufactured for: Auromedics Pharma LLC 6 Wheeling Road Dayton NJ 08810, Made in India. NDC 55150-120-30

Reason for recall

Presence of Particulate Matter: identified as glass and silicone material

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-1030-2018
Date reported July 18, 2018
Date initiated July 2, 2018
Recalling firm AuroMedics Pharma LLC
Firm location East Windsor, NJ
Affected scope 73620 single-dose vials
Distribution Nationwide in the USA

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-1030-2018) 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 3.375 grams per vial, Single-Dose Vial, Rx Only. Manufactured for: Auromedics Pharma LLC 6 Wheeling Road Dayton NJ 08810, Made in India. NDC 55150-120-30. Recalled by AuroMedics Pharma LLC. Units affected: 73620 single-dose vials.
Why was this product recalled?
Presence of Particulate Matter: identified as glass and silicone material
Which agency issued this recall?
This recall was issued by the FDA Drug on July 18, 2018. Severity: Critical. Recall number: D-1030-2018.
Where was the recalled product distributed?
Distribution: Nationwide in the USA.
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.

Similar severity · nearest report date

Same archive severity grade (Critical), closest by report date among other firms and states.

Similar Drugs & Medications · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Compare this recall with Kian Pee Wan Capsules, 30-count bottles → · All Drugs & Medications recalls

This recall: FDA Drug, reported July 18, 2018. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026