CLASS II Drug recall · Reported 11 May 2022 · FDA Enforcement Report

Vancomycin HCl in 0.9% Sodium Chloride recalled by SCA Pharmaceuticals

SCA Pharmaceuticals is recalling Vancomycin HCl in 0.9% Sodium Chloride, distributed nationwide in the US. The recall was initiated on 25 Apr 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 1222035839, Exp. Date 09-Aug-22
Quantity recalled30 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-0831-2022
FDA event ID
90080
Recalling firm
SCA Pharmaceuticals, Windsor, CT
Classification
Class II
Status
Terminated
Recall initiated
25 Apr 2022
FDA classified
2 May 2022
Reported
11 May 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Antibiotics

Timeline

25 Apr 2022Recall initiated by company
2 May 2022Classified by FDA+7 days
11 May 2022Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations

Product as listed by the FDA

Vancomycin HCl 1.5 g in 0.9% Sodium Chloride, 500 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0924-44

Where it was distributed

Product was distributed nationwide within the United States

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations

Which lots are affected?

Lot #: 1222035839, Exp. Date 09-Aug-22

Where was it sold?

Product was distributed nationwide within the United States

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

2 other products · FDA event 90080

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