Par Health recall: Buprenorphine Hydrochloride
Par Health USA, LLC is recalling Buprenorphine Hydrochloride – 154210 bottles. The U.S. Food and Drug Administration published the recall on October 7, 2026; it began on September 8, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Buprenorphine Hydrochloride |
| Brand | Par Health |
| Company | Par Health USA, LLC |
| Type | Drugs |
| Classification | Class II |
| Recall date | September 8, 2026 |
| Published by FDA | October 7, 2026 |
| Quantity | 154210 bottles |
| Recall ID | 99902 |
Recalled products
- Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05
- FDA recall number
- D-0876-2026
- Codes, lots and dates
- Lot#:83912, Exp Date 10/2026 Lot#:84234, Exp Date 11/2026 Lot#:84990, Exp Date 11/2026 Lot#:85003, Exp Date 12/2026 Lot#:86443, Exp Date 01/2027 Lot#:89909, Exp Date 05/2027
- Quantity
- 154210 bottles
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99902
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Rochester, MI, United States
Why it was recalled
The reason the FDA lists: “Crystallization”
Where it was sold
Nationwide. Distribution as the FDA records it: “U.S. Nationwide”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99902, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other drug recalls
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|---|---|---|---|
| Oct 7, 2026 |  Ajanta Pharma recall: Ranolazine Extended-Release TabletsDrugs | Failed Dissolution Specifications: below specification Serious | FDA Class II |
| Oct 7, 2026 | Apotex recall: Paroxetine Extended-Release TabletsDrugs | Failed dissolution specifications. Serious | FDA Class II |
| Oct 7, 2026 | TerSera Therapeutics recall: ZoladexDrugs · 296 cartons | Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient ou… Serious | FDA Class II |
| Oct 7, 2026 | Aurolab Trust recall: FOCUS PI Hypromellose 0.7% FormulaDrugs · 25,220 bottles | a sterility problem Serious | FDA Class II |
| Oct 7, 2026 | Amneal Pharmaceuticals recall: Estradiol GelDrugs · 2,592 30-count cartons | Defective Container; packets were found to be either empty or partially full. Serious | FDA Class II |
| Oct 7, 2026 | SV Labs Toronto recall: Benzoyl Peroxide WashDrugs | microbial contamination Serious | FDA Class II |
About this recall
Is Par Health Buprenorphine Hydrochloride recalled?
Yes. Par Health USA, LLC recalled it on September 8, 2026; FDA published it October 7, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Crystallization
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.