Boss Instruments recalls specific endoscopic needle holders due to tungsten carbide plate breaking under pressure, potentially causing needle slippage during procedures.
The tungsten carbide plate, which is intended to hold the sewing needle securely, can break when holding the sewing needle under pressure.
Boss Instruments is recalling certain endoscopic needle holders because the tungsten carbide plate that holds the sewing needle can break when pressure is applied. This could lead to the needle slipping during use, which might cause injury.
The needle holder's tungsten carbide plate can break when pressure is applied to the sewing needle. This breakage may cause the needle to slip, potentially leading to injury during endoscopic procedures.
Endoscopists and medical professionals who use the recalled needle holders for endoscopic procedures are most at risk. Patients undergoing these procedures could be affected if the needle slips.
Check for part numbers 50-2503 or 51-2503 on the needle holders. These are used in endoscopic procedures and were sold with specific lot numbers listed in the recall notice.
Identify the part numbers (50-2503 or 51-2503) and lot numbers (e.g., 00351415) to confirm if your needle holder is recalled.
The tungsten carbide plate that holds the sewing needle can break under pressure, potentially causing the needle to slip during endoscopic procedures.
Check the part numbers and lot numbers listed in the recall notice to determine if your product is affected. If it is, contact Boss Instruments for further instructions.
Yes, the needle could slip if the plate breaks, which might cause injury during endoscopic procedures.
We’ve drafted a message you can send Boss Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-2767-2020 — Boss Instruments Boss Instruments Hello, I own a Boss Instruments that is covered by recall Z-2767-2020 from Boss Instruments. 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.
