--- title: "STAQ Pharma, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search STAQ Pharma, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/staq-pharma-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # STAQ Pharma, Inc. recall records **3** reported ongoing 6 records in this archive. Latest source date Oct 9, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Oct 9, 2025 FDA drug enforcement ### [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.](https://isitonrecall.com/recall/fda-drug-d-0023-2026-hydromorphone-hcl-pf-10mg-50-ml-0-2mg-ml-in-nacl-injection-for-iv-use-50-ml-syringe-staq-pharma-inc/) Labeling: Incorrect or Missing Lot and/or Exp Date Class III Reported ongoing Distribution: Nationwide in the U.S. [Official source for Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Ph...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0023-2026%22) Oct 9, 2025 FDA drug enforcement ### [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.](https://isitonrecall.com/recall/fda-drug-d-0024-2026-ketamine-hydrochloride-50mg-5-ml-10mg-ml-injection-for-iv-use-50-ml-syringe-staq-pharma-inc-14135-e/) Labeling: Incorrect or Missing Lot and/or Exp Date Class III Reported ongoing Distribution: Nationwide in the U.S. [Official source for Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0024-2026%22) Oct 9, 2025 FDA drug enforcement ### [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.](https://isitonrecall.com/recall/fda-drug-d-0025-2026-fentanyl-citrate-pf-500mcg-50-ml-10mcg-ml-in-nacl-injection-for-iv-use-50-ml-syringe-staq-pharma-inc/) Labeling: Incorrect or Missing Lot and/or Exp Date Class III Reported ongoing Distribution: Nationwide in the U.S. [Official source for FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ P...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0025-2026%22) Nov 29, 2023 FDA drug enforcement ### [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 Inc. 14135 E 42nd Ave, Unit 50, Denver, Colorado 80239, NDC...](https://isitonrecall.com/recall/fda-drug-d-0147-2024-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 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... Class II Reported completed Distribution: Nationwide within the United States [Official source for ROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) Injection, 500 mL bags, ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0147-2024%22) Feb 3, 2022 FDA drug enforcement ### [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., Denver, CO 80239, NDC: 73177-0104-05.](https://isitonrecall.com/recall/fda-drug-d-0633-2022-hydromorphone-hcl-pf-10-mg-50-ml-0-2mg-ml-in-nacl-50-ml-in-50-ml-single-dose-syringe-rx-only-staq-ph/) Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A Class I Reported terminated Distribution: CO, OH, and TX. [Official source for HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0633-2022%22) Feb 3, 2022 FDA drug enforcement ### [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, CO 80239, NDC: 73177-0105-04.](https://isitonrecall.com/recall/fda-drug-d-0634-2022-morphine-sulfate-pf-25-mg-25ml-1-mg-ml-in-nacl-25-ml-in-30-ml-single-dose-syringe-rx-only-staq-pharm/) Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A Class I Reported terminated Distribution: CO, OH, and TX. [Official source for Morphine Sulfate PF 25 mg/25mL (1 mg/mL) in NaCl, 25 mL in 30 mL Single Dose Syringe, Rx only, ST...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0634-2022%22) ## Reasons in these listed records - Labeling: Incorrect or Missing Lot and/or Exp Date - 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. - Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A These examples come from this result page and are not a ranking of every recall reason. ## Checking STAQ Pharma, Inc. ### Is there a recall on staq pharma, inc. right now? This archive contains 6 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search STAQ Pharma, Inc.](https://isitonrecall.com/check/?q=STAQ%20Pharma%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)