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.
Reported: October 22, 2025 Initiated: October 9, 2025 #D-0023-2026
Product Description
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.
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp Date
Details
- Recalling Firm
- STAQ Pharma, Inc.
- Distribution
- Nationwide in the U.S.
- Location
- Denver, CO
Frequently Asked Questions
What product was 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.. Recalled by STAQ Pharma, Inc..
Why was this product recalled? ▼
Labeling: Incorrect or Missing Lot and/or Exp Date
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 22, 2025. Severity: Low. Recall number: D-0023-2026.
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