DJO Surgical recalls reverse shoulder system components due to potential infection from unsterilized parts. Affected items include specific semi-humeral socket inserts and baseplates with serial numbers ending in 00888912024693, 00888912024754, and 00888912024754.
Orthopedic device components were not subjected to final sterilization before shipment, which if implanted may lead to varying degrees of infection, which may require treatment, prolonged monitoring, and may lead to revision surgery
DJO Surgical is recalling certain reverse shoulder system components because they were not properly sterilized before shipping. If implanted, these parts could cause infections requiring treatment, monitoring, and possible surgery.
The components were not sterilized before shipment, which means they could carry harmful bacteria. If implanted, this could lead to infections that require antibiotics, additional surgeries, or long-term monitoring.
Patients who received the recalled reverse shoulder system components during surgery are most at risk. The recall affects specific models and serial numbers used in orthopedic procedures.
Check the serial numbers on the product labels: 508-01-032 (ending with 00888912024693), 508-32-104 (ending with 00888912024754), and 508-36-101 (ending with 00888912024754). These parts were sold between April 2027 and May 2029.
Look for serial numbers ending in 00888912024693, 00888912024754, or 00888912024754 on the product labels.
The components were not sterilized before shipment, which could lead to infections if implanted.
The recall record does not specify a remedy, so contact DJO Surgical directly for guidance.
Yes, the recalled models include the 32mm semi-humeral socket insert (REF: 508-01-032) and baseplates with specific serial numbers.
We’ve drafted a message you can send DJO Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2606-2023 — DJO Surgical DJO Surgical Hello, I own a DJO Surgical that is covered by recall Z-2606-2023 from DJO Surgical. 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.
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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.
