Trilliant Surgical recalls specific cannulated driver handles (210-00-003) that may have adapter collar sticking or failing to retain the mating adapter. This affects medical devices used in surgery.
Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.
Trilliant Surgical is recalling a specific type of surgical device (cannulated driver handle) that may cause the adapter collar to stick or fail to hold the mating adapter. This could lead to improper function during surgery.
The adapter collar may stick or fail to retain the mating adapter shaft, which could cause improper function during surgical procedures. This might lead to incorrect device positioning or movement, potentially affecting the procedure's safety and effectiveness.
Surgical professionals using the recalled cannulated driver handle (model 210-00-003) for procedures requiring non-sterile, prescription-only medical devices. Patients at risk are those undergoing surgery with this specific device.
Check for the product name 'Cannulated Driver Handle' with catalog number 210-00-003. The device is sold as a prescription-only, non-sterile medical device for surgical use.
Verify the catalog number on the device; if it is 210-00-003, it is affected.
The recall states the device may have adapter collar sticking or failing to retain the mating adapter, so it is not recommended for use until the recall is addressed.
The recall does not specify a remedy, so contact Trilliant Surgical directly for guidance.
Look for the catalog number 210-00-003 on the device, which is a prescription-only, non-sterile surgical device.
We’ve drafted a message you can send Trilliant Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2338-2018 — Trilliant Surgical Trilliant Surgical Hello, I own a Trilliant Surgical that is covered by recall Z-2338-2018 from Trilliant 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.
