Par Health USA recalls specific buprenorphine injections due to crystallization risk. This may affect patients using these medications. Contact your healthcare provider for guidance.
Crystallization; identified as Buprenorphine free base
Par Health USA is recalling certain buprenorphine injections because they may crystallize, potentially causing safety issues. This recall affects patients using these medications under prescription.
The buprenorphine injections may crystallize, which could lead to improper drug delivery or other safety concerns. This crystallization is identified as buprenorphine free base. The exact risk level and potential harm are not clearly described in the recall notice.
Patients prescribed buprenorphine injections by a healthcare provider. Those using the specific product with the listed lot numbers are most at risk.
Check for the product name: Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton. Look for lot numbers 82886 (expiring 09/30/2026) or 89646 (expiring 05/31/2027).
Reach out to your prescribing doctor or healthcare provider for guidance on next steps.
The recall does not specify if the product is safe to use. The hazard is described as crystallization risk, but the exact safety implications are unclear.
The recall does not provide a specific remedy. Contact your healthcare provider for guidance.
Check for the product name and lot numbers 82886 (expiring 09/30/2026) or 89646 (expiring 05/31/2027).
We’ve drafted a message you can send Par Health to request your refund or repair — edit it as you like.
Subject: Recall D-0596-2026 — Par Health Par Health Hello, I own a Par Health that is covered by recall D-0596-2026 from Par Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.