CLASS II Drug recall · Reported 6 Jan 2016 · FDA Enforcement Report
Piperacillin/Tazobactam (Zosyn) Accuflo, a)/NS b)/NS Accuflo recalled
Walgreens Infusion Services is recalling Piperacillin/Tazobactam (Zosyn) Accuflo, a)/NS b)/NS Accuflo, distributed in Texas. The recall was initiated on 10 Nov 2015 and the FDA has classified it as Class II.
Check your package
Lot, batch or date codes All lots within expiry.
Quantity recalled 26 Accuflo bags
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
Recall number D-0529-2016
FDA event ID 72594
Classification Class II
Status Terminated
Recall initiated 10 Nov 2015
FDA classified 30 Dec 2015
Reported 6 Jan 2016
Type Voluntary: Firm initiated
Customers notified by Letter
Timeline
10 Nov 2015 Recall initiated by company 30 Dec 2015 Classified by FDA +50 days 6 Jan 2016 Published in enforcement report +7 days
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Assurance of Sterility
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Piperacillin/Tazobactam (Zosyn) Accuflo bag, a) 18 g/NS 275 mL b) 4.5 g/NS 100 mL Accuflo, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Questions about this recall
Why was it recalled? Lack of Assurance of Sterility
Which lots are affected? All lots within expiry.
Where was it sold? Texas
What should I do if I have it? Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean? Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event 32 other products · FDA event 72594 This product is part of a recall event; the main page for the event is 0.9% NaCl with Ca 4.65 meq recalled by Walgreens Infusion Services .
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