DJO Surgical Recalls

4 recalls found for DJO Surgical. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

DJO Surgical ALTIVATE Glenoid Reamer Head Recall Expands to 927 Units

DJO Surgical recalled 927 ALTIVATE reverse wedge glenoid reamer heads distributed nationwide in the United States after concerns that the devices may kick or bind up during use. The issue involves model 804-06-311 and non-sterile stainless steel material. Healthcare providers and patients should stop using the device immediately and contact Encore Medical, LP for instructions.

DJO Surgical
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Health & Personal Care
HIGH
FDA DEVICE

DJO Surgical Recalls 447 ALTIVATE Reverse Glenoid Reamer Sleeve Units (2025)

DJO Surgical is recalling 447 ALTIVATE Reverse Glenoid Reamer Sleeve devices distributed nationwide in the United States. The device may kick or bind up during or immediately prior to use. Healthcare providers and patients should stop using the device and follow recall instructions issued by Encore Medical, LP via email.

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Brand Statistics

Total Recalls
4
Pages
1

Related Brands

EnovisEncore Medical