Home / Recalls / AuroMedics Pharma LLC / D-0926-2018

D-0926-2018 Class I Terminated

Recalled by AuroMedics Pharma LLC — East Windsor, NJ

FDA drug recall D-0926-2018 was initiated by AuroMedics Pharma LLC on May 1, 2018 and is designated Class I. Reason for recall: Presence of Particulate Matter: confirmed customer report for presence of visible particulate matter, confirmed as glass The recall status is terminated (terminated Jun 21, 2023). Affected quantity: 77,400 vials.

Recall Details

Product Type: Drugs
Report Date: May 23, 2018
Initiation Date: May 1, 2018
Termination Date: Jun 21, 2023
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 77,400 vials

Product Description

Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, For Intravenous Use Only, Single-Dose vial, Rx Only, Manufactured for: AuroMedics Pharma LLC, 6 Wheeling Road, Dayton, NJ 05610. NDC 55150-120-30

Reason for Recall

Presence of Particulate Matter: confirmed customer report for presence of visible particulate matter, confirmed as glass

Distribution Pattern

Nationwide in the USA

Code Information

Lot #s: PP0317061-A, PP0317049-A; EXP August 2019

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0926-2018
openFDA file date: Oct 6, 2026
Loaded by RegDataLab: Oct 12, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.

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