T.A.G. Medical recalls Betta Link LG Reusable Pronged Guides due to potential metal shavings from bending during surgery, risking patient injury. Affected units include specific lot numbers.
Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes potential of injury.
T.A.G. Medical is recalling Betta Link LG Reusable Pronged Guides that could bend during surgery, potentially causing metal shavings that might injure patients. This recall affects specific lot numbers and requires immediate attention to prevent harm.
The drill guides might bend when axial forces are applied by the surgeon during surgery. This bending can cause metal shavings due to friction with the drill bit, which may injure patients.
Surgeons using the Betta Link LG Reusable Pronged Guides for soft tissue to bone fixation in surgeries are most at risk. Patients undergoing procedures with these guides could face injury from metal shavings.
Check for part number 110045156 or UDI-DI 10818674025819. Affected units include lot numbers 22A01, 22C01, and 22F01.
Verify your Betta Link LG Reusable Pronged Guide has part number 110045156 or UDI-DI 10818674025819 with lot numbers 22A01, 22C01, or 22F01.
The drill guides might bend during surgery, causing metal shavings that could injure patients.
Check for part number 110045156 or UDI-DI 10818674025819 with lot numbers 22A01, 22C01, or 22F01.
The recall record does not specify a remedy, so contact T.A.G. Medical for guidance.
We’ve drafted a message you can send T.A.G. Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2064-2023 — T.A.G. Medical T.A.G. Medical Hello, I own a T.A.G. Medical that is covered by recall Z-2064-2023 from T.A.G. Medical. 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.
