Stryker recalls Endotrig ETF Hook Blade (Catalog 1052-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected lots: 01406, 01475.
The seal integrity of the sterile bag containing the kits may be compromised.
Stryker is recalling Endotrig ETF Hook Blade surgical kits because the sterile packaging might not stay sealed properly. This could lead to infections if the kit is used without a clean seal.
The sterile bag containing the surgical kits might not stay sealed properly. If the seal is broken, the kit could become contaminated and cause infection during surgery.
Surgical patients and medical professionals using the Endotrig ETF Hook Blade with lot numbers 01406 or 01475. Those at highest risk are patients undergoing plantar fasciosis treatment.
Check the lot number on the packaging. The affected items have lot numbers 01406 or 01475. The product is the Endotrig ETF Hook Blade with catalog number 1052-1.
Look for lot numbers 01406 or 01475 on the packaging.
The sterile bag containing the kits may have compromised seal integrity, which could lead to contamination and infection risk during surgery.
Check the lot number on the packaging. If it's 01406 or 01475, contact Stryker for instructions.
The recall is for potential infection risk, not direct injury. The hazard does not involve death or serious injury in normal use.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2412-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2412-2019 from Stryker. 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.
