Medtronic recalls specific scalp clip kits due to inadequate packaging performance. Affected models and lots may not meet current safety standards. Consumers should check their product details and follow official instructions.
Medtronic is initiating a voluntary recall because the products identified above did not adequately demonstrate acceptable packaging performance to current standards.
Medtronic is recalling two specific scalp clip kit models (CG8900 and CG8901) because their packaging did not meet current safety standards. This means the products could be unsafe if the packaging fails during use, though no injuries have been reported.
The packaging in these scalp clip kits did not meet current safety standards, which could lead to the products failing during use. This might cause the clips to not function properly, but there is no indication of injury or serious harm from this issue.
People who own or use Medtronic scalp clip kits with the model numbers CG8900 or CG8901, and the listed lots. Medical professionals using these kits for procedures are most at risk.
Check for model numbers CG8900 or CG8901 on the product. The affected lots are listed in the recall notice, including codes like D80412, D84100, and E00008. These kits were sold in the U.S. between specific dates.
Look for model numbers CG8900 or CG8901 and the affected lots listed in the recall notice.
Medtronic is recalling these scalp clip kits because their packaging did not meet current safety standards.
No, the recall is for packaging performance, not a safety hazard. You can continue using them as long as you check the model and lot numbers.
Check the model number (CG8900 or CG8901) and the lot number against the list provided in the recall notice.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0622-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0622-2018 from Medtronic. 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.
