Medtronic recalls biopsy needle kits with potential depth stop issues that could delay surgery. Affected units include specific product numbers and lot numbers.
The firm has become aware that due to a manufacturing issue impacting the biopsy needle depth stop, there exist the potential that some biopsy needle depth stops, when tightened, may not securely tighten to the biopsy needle. This could result in a delay in surgery.
Medtronic is recalling biopsy needle kits that may not securely tighten, potentially delaying surgery. This issue affects specific product numbers and lot numbers sold to medical users.
The biopsy needle depth stop may not tighten securely when the kit is assembled. This could lead to delays in surgical procedures if the needle does not hold properly during use.
Medical professionals using the recalled biopsy needle kits are most at risk. The recall targets specific product numbers and lot numbers sold to hospitals and clinics.
Check for product number 9736075 and lot numbers 0009754921, 0009921274, 0009940846, 0009921273, 0009921276, or 0009952564 on the kit packaging.
Verify the product number and lot numbers listed on the kit packaging to confirm if it is affected.
The recall indicates a potential for delayed surgery, but the risk of serious injury is not described. The hazard is low risk as it does not involve immediate danger.
Check for product number 9736075 and lot numbers 0009754921, 0009921274, 0009940846, 0009921273, 0009921276, or 0009952564 on the kit packaging.
The recall does not specify a remedy, so contact Medtronic Navigation directly for guidance.
We’ve drafted a message you can send Medtronic Navigation to request your refund or repair — edit it as you like.
Subject: Recall Z-0659-2020 — Medtronic Navigation Medtronic Navigation Hello, I own a Medtronic Navigation that is covered by recall Z-0659-2020 from Medtronic Navigation. 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.
