STAQ Pharma, Inc.: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: February 23, 2022. Most recent: October 22, 2025.

Risk classification: Class I: 2 · Class II: 1 · Class III: 3

Most recent recalls

DateAgencyProduct
October 22, 2025FDAHydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe,…D-0023-2026
October 22, 2025FDAFentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe…D-0025-2026
October 22, 2025FDAKetamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Ph…D-0024-2026
December 13, 2023FDAROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) Injection, 500 m…D-0147-2024
February 23, 2022FDAMorphine Sulfate PF 25 mg/25mL (1 mg/mL) in NaCl, 25 mL in 30 mL Single Dose Syringe, Rx …D-0634-2022
February 23, 2022FDAHYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, …D-0633-2022

Questions about this company

How many recalls does STAQ Pharma, Inc. have?
Recalert has 6 U.S. recalls on record for STAQ Pharma, Inc., published between February 23, 2022 and October 22, 2025.
What was the most recent STAQ Pharma, Inc. recall?
FDA recall D-0023-2026, published October 22, 2025: 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.
Which agencies have handled STAQ Pharma, Inc. recalls?
STAQ Pharma, Inc. appears as the recalling firm in recalls from: FDA (6).

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