SCA Pharmaceuticals recalls specific Hydro Morphone HCl syringes due to lack of sterility assurance. Affected lots expire by November 2023. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling certain Hydro Morphone HCl syringes because they may not be sterile. This could lead to infections if used improperly. The recall affects specific lots with expiration dates up to November 2023.
The syringes may not be sterile, which could cause infections if used for injections. This is a serious risk because medical injections require sterile conditions to prevent contamination.
Prescription users of Hydro Morphone HCl 6 mg/30 mL syringes from SCA Pharmaceuticals. Patients who have the specific lots listed in the recall are most at risk.
Check the lot numbers on the syringe: 1223048451 (expires 11/20/23), 1223048923 (expires 12/07/23), 1223049097 (expires 12/15/23), or 1223049129 (expires 12/19/23). The product is only available by prescription.
Look for the lot numbers listed in the recall: 1223048451, 1223048923, 1223049097, or 1223049129.
The recall is for lack of assurance of sterility, which could lead to infections if used improperly.
Contact SCA Pharmaceuticals at 755 Rainbow Rd., Windsor, CT 06095 for details on the remedy.
Check the lot numbers: 1223048451 (expires 11/20/23), 1223048923 (expires 12/07/23), 1223049097 (expires 12/15/23), or 1223049129 (expires 12/19/23).
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0406-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0406-2024 from SCA Pharmaceuticals. 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.