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Health & beauty United States Recall (ongoing)

STAQ Pharma, Inc. recalls Hydromorphone HCL PF and 2 more products

Hydromorphone HCL PF 10 mg/50 mL (0.2 mg/mL) in 50 mL syringe (NDC 73177-0104-05), Ketamine Hydrochloride 50 mg/5 mL (10 mg/mL) in 50 mL syringe (NDC 73177-0156-02), and FentaNYL Citrate PF 500 mcg/50 mL (10 mcg/mL) in 50 mL syringe (NDC 73177-0102-05) from STAQ Pharma, Inc. are included in this recall; affected lots include 25104595A (exp 27DEC2025), 25156673A (exp 02FEB2026), 25102464B (exp 26NOV2025), 25102370A (exp 20OCT2025), and 25102369A (exp 19OCT2025). They were recalled because of incorrect or missing lot and/or expiration date labeling and were sold nationwide in the U.S.

What's being recalled

Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0104-05.

Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0156-02.

FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0102-05.

Recalling firm: STAQ Pharma, Inc., Denver, CO, United States.

How to identify it

Lot #: 25104595A, Expiry: 27DEC2025. Lot #: 25156673A, Expiry: 02FEB2026. Lot: 25102464B, Expiry: 26NOV2025; 25102370A, Expiry: 20OCT2025; 25102369A, Expiry: 19OCT2025.

The hazard

Labeling: Incorrect or Missing Lot and/or Exp Date

What to do

Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.

The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.

Where it was sold

Nationwide in the U.S.

The official notice

This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.

Read the official notice (opens in a new tab)

A little guidance

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