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Food & drug recall · FDAMarch 12, 2024Serious

Hikma Pharmaceuticals USA Inc. — Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only

Do not stop taking this without speaking to your pharmacist or doctor.

What’s wrong

The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.

The Recall Registry rates this serious — FDA Class II: temporary or medically reversible health harm.

What to do

Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.

Who to contact: Recalling firm: Hikma Pharmaceuticals USA Inc.

The product

Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01

Details

Units affected
22,644 ampuls
Recall date
March 12, 2024
Brand
Hikma Pharmaceuticals USA Inc.
Model, lot or SKU numbers
Lot #: 052001, 052003, Exp. Date 11/2024023012, 023014, Exp. Date 08/2024
Where it was distributed

Nationwide within the United States

The official notice

This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.

Their exact wording: “Hikma Pharmaceuticals USA Inc. — Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx only, Manufactured by Hikma Berkeley Heights, NJ 07922, NDC 0641-6039-01”

Read it on FDA →

Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.

Filed under: Prescription medicine

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