Reported Jun 22, 2022 · Terminated
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Manufactured for:…
Sun Pharmaceutical Industries Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: SUN PHARMACEUTICAL INDUSTRIES INC · 2 Independence Way · Princeton, NJ · 08540-6620
Is this the product you have?
- medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only
- Manufactured forNorthstart Rx LLC, Memphis, TN, 38141
- Manufactured bySun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC 16714-981-01
- Lot codes and dates
11 of 11 products
Products covered by this recall # Product as published 1 Lot: HAC2075A, Exp 06/2023 2 HAC2076A, Exp 07/2023 3 HAC2077A, HAC2078A, Exp 08/2023 4 HAC3803A, Exp 09/2023 5 HAC0551A, Exp 02/2023 6 HAC0562A, HAC1183A, Exp 03/2023 7 HAC1807A, Exp 06/2023 8 JKX6017A, JKX6018A Exp 12/2022 9 HAC0163A, Exp 01/2023 10 HAC1184A, Exp 04/2023 11 HAC0162A, Exp 12/2022. - Amount recalled
- 180813 syringes
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
Lack of assurance of sterility
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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