T.A.G. Medical recalls Betta Link SR reusable fishmouth guides due to potential metal shavings from bending during surgery. Affected units include specific lot numbers and part numbers for soft tissue to bone fixation procedures.
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 SR reusable fishmouth guides used in soft tissue to bone fixation surgeries. The guides might bend during use, causing metal shavings that could injure patients. This recall affects specific lot numbers and part numbers.
The drill guides can bend when axial forces are applied by surgeons during procedures. This bending may cause metal shavings due to friction with the drill bit, which could lead to patient injury.
Surgical teams using the Betta Link SR fishmouth guides for soft tissue to bone fixation procedures are most at risk. Patients undergoing these surgeries with the affected units may face injury from metal shavings.
Check for part number 110045151 and lot numbers 22A01, 22C01, or 22C02 on the product. The guides are intended for soft tissue to bone fixation in ligament or tendon repairs.
Verify the part number (110045151) and lot numbers (22A01, 22C01, 22C02) on the Betta Link SR fishmouth guide.
The guides might bend during surgery, causing metal shavings that could injure patients.
Lot numbers 22A01, 22C01, and 22C02.
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-2063-2023 — T.A.G. Medical T.A.G. Medical Hello, I own a T.A.G. Medical that is covered by recall Z-2063-2023 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.
