Par Sterile Products LLC recalls
Every recall we track for Par Sterile Products LLC — 4 in all, from 2017–2024 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Par Sterile Products LLC 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 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 1 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 1 | 1 | 0 | 0 | 2 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Par Sterile Products LLC 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 Par Sterile Products LLC recalls
4 shown- Use cautionDrug
Par Sterile Products LLC recalls Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial,
Par Sterile Products recalls Treprostinil Injection 20 mg/20 mL vials due to potential particulate matter. This could cause serious complications during infusion. Consumers should contact the manufacturer for details.
Par Sterile ProductsMar 4, 2024 - Stop using nowDrug
Par Sterile Products LLC recalls Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose
Par Sterile Products recalls Vasostrict (vasopressin) injections due to potential overdose risk from assay exceeding stability limits. This affects specific lot numbers and expiration dates.
Par Sterile ProductsJan 11, 2024 - UnratedDrug
PAR Sterile Products LLC recalls Buprenorphine HCl, Injection, 0.3mg/mL, For Intramuscular or Intravenous Use, Rx Only, 1mL Single Dose Vial, (supplied
Par Sterile Products recalls buprenorphine injections that may crystallize, causing potential safety issues. This recall affects specific lots manufactured between 2021 and 2023.
Par Sterile ProductsNov 9, 2021 - Lower riskDrug
PAR Sterile Products LLC recalls Buprenorphine HCI Injection, 0.3 mg/mL, 1 mL Single Dose Vial (NDC 42023-179-01), packaged in 1 mL x 5 Single Dose
Par Sterile Products recalls buprenorphine injections with crystalline particulates that could cause injection site reactions. Affected lots from 2018-01 to 2018-10 are included in this recall.
Par Sterile ProductsApr 28, 2017
Par Sterile Products LLC recall questions
How many recalls has Par Sterile Products LLC had?
4 recalls from Par Sterile Products LLC are on record with U.S. safety agencies, from 2017–2024.
What is the most recent Par Sterile Products LLC recall?
Par Sterile Products LLC recalls Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial,, dated Mar 4, 2024. Every Par Sterile Products LLC recall is listed on this page, newest first.
What should I do if I have a recalled Par Sterile Products LLC 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 Par Sterile Products LLC 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.