Applied Medical Resources Corp recalls Kii Low Profile Bladed Dual Pack (REF: CTB23) due to potential blade obturator extension after assembly, which could cause injury.
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Applied Medical Resources Corp is recalling Kii Low Profile Bladed Dual Pack surgical devices because the blade obturator might extend too far after assembly, creating a risk of injury during use.
The blade obturator may extend beyond the intended length after assembly into the cannula and seal housing. This could cause the blade to become too long and potentially injure the user or patient during medical procedures.
Surgical professionals and hospitals using the Kii Low Profile Bladed Dual Pack (REF: CTB23) are affected. Those handling the devices during procedures are at the highest risk.
Check for the Kii Low Profile Bladed Dual Pack with REF: CTB23, UDI: (01)00607915126582, and Lot # 1546141. This product was sold in the U.S. and used in medical settings.
Verify the product's reference number (REF: CTB23), unique device identifier (UDI: (01)00607915126582), and lot number (1546141) to confirm it is recalled.
The recall indicates a potential risk of the blade obturator extending too far after assembly, which could cause injury. However, the hazard is not described as causing serious injury in normal use.
The recall does not specify a remedy, so no action is required beyond checking if your product matches the recall details.
Look for the Kii Low Profile Bladed Dual Pack with REF: CTB23, UDI: (01)00607915126582, and Lot # 1546141.
We’ve drafted a message you can send Applied Medical Resources Corp to request your refund or repair — edit it as you like.
Subject: Recall Z-1010-2026 — Applied Medical Resources Corp Applied Medical Resources Corp Hello, I own a Applied Medical Resources Corp that is covered by recall Z-1010-2026 from Applied Medical Resources Corp. 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.
