STAQ Pharma, Inc. recalls
Every recall we track for STAQ Pharma, Inc. — 6 in all, from 2022–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from STAQ Pharma, Inc. peaked in 2025 (3); 6 since 2017.
All FDA recall records for STAQ Pharma, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 2 | 0 | 2 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 3 | 0 | 3 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for STAQ Pharma, Inc. recalls
What to do if you have a recalled STAQ Pharma, Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All STAQ Pharma, Inc. recalls
3 shown- Lower riskDrug
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,
STAQ Pharma recalls 50mL ketamine IV injection with missing lot or expiration date. Patients should check labels for correct dates to avoid medication errors.
STAQ PharmaOct 9, 2025 - Lower riskDrug
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
STAQ Pharma recalls 500mL ROPivacaine HCl 0.2% injection bags with leaking issues. These bags were manufactured by a third party and failed quality checks. Consumers should check lot numbers on the packaging.
STAQ PharmaNov 29, 2023 - Lower riskDrug
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.,
STAQ Pharma recalls 50mL single-dose hydro morphine syringes with incorrect morphine sulfate labeling. This could lead to medication errors if used without proper identification.
STAQ PharmaFeb 3, 2022
STAQ Pharma, Inc. recall questions
How many recalls has STAQ Pharma, Inc. had?
6 recalls from STAQ Pharma, Inc. are on record with U.S. safety agencies, from 2022–2025.
What is the most recent STAQ Pharma, Inc. recall?
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,, dated Oct 9, 2025. Every STAQ Pharma, Inc. recall is listed on this page, newest first.
Why are STAQ Pharma, Inc. products recalled?
The most common reasons on record: Labeling: Incorrect or Missing Lot and/or Exp Date (3).
What should I do if I have a recalled STAQ Pharma, Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new STAQ Pharma, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.