STAQ Pharma Recalls
6 recalls on record · February 23, 2022 to October 22, 2025 · Drugs
Recalls by year
22
23
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 22, 2025DrugsFDA
STAQ Pharma, Inc. recalls FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42n
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
October 22, 2025DrugsFDA
STAQ Pharma, Inc. recalls Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, De
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
October 22, 2025DrugsFDA
STAQ Pharma, Inc. recalls Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Pharma Inc., 14135 E 42nd
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
December 13, 2023DrugsFDA
STAQ Pharma, Inc. recalls ROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) Injection, 500 mL bags, Rx only, STAQ Pharma In
Hazard: STAQ Pharma Inc. received consumer complaints related to leaking bags and other potential bag concerns. Upon investigation, they determine the source of the issue was with the bag manufacturer who released bags Lot # 134142-001A which had failed internal QC tests for leaks.
February 23, 2022DrugsFDA
STAQ Pharma, Inc. recalls Morphine Sulfate PF 25 mg/25mL (1 mg/mL) in NaCl, 25 mL in 30 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver
Hazard: Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A
February 23, 2022DrugsFDA
STAQ Pharma, Inc. recalls HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Den
Hazard: Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A