Ad-Tech Medical recalls disposable drill kits with possible mix-up of 2.4mm and 2.8mm drill bits. These kits are used for cranial surgery and may cause errors if used incorrectly.
There is a possibility that DDK2-2.4-30X Disposable Drill Kits, Lot Number 111664 208140649 contained 2.8mm drill bits from DDK2-2.8-30X Disposable Drill Kits, Lot Number 111745 208140649 and vice versa.
Ad-Tech Medical is recalling disposable drill kits that could have mixed 2.4mm and 2.8mm drill bits. This mix-up might lead to incorrect drilling during cranial surgery, which could cause complications.
The drill kits may contain the wrong bit size (2.4mm instead of 2.8mm or vice versa) due to a mix-up in production. This could lead to incorrect drilling during cranial surgery, potentially causing complications.
Medical professionals using these drill kits for cranial procedures are most at risk. Patients undergoing surgery with these kits could face complications due to incorrect bit sizes.
Check for the product name 'Disposable Drill Kit' with catalog numbers DDK2-2.4-30X (Lot 0111664 208140649) or DDK2-2.8-30X (Lot 0111745 208140649).
Look for the catalog number and lot number on the kit to confirm if it's affected.
The recall is due to a possible mix-up between 2.4mm and 2.8mm drill bits in the kits, which could lead to incorrect drilling during cranial surgery.
The official notice does not specify a remedy, so check the catalog number and lot number to see if it's affected.
The recall is for medical use only; patients are not directly affected unless the kit is used incorrectly during surgery.
We’ve drafted a message you can send Ad-Tech Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1938-2018 — Ad-Tech Medical Ad-Tech Medical Hello, I own a Ad-Tech Medical that is covered by recall Z-1938-2018 from Ad-Tech 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.