Stryker recalls specific lot numbers of T5 Zipper Toga with Peel-Away Face Shield for potential contaminant exposure due to material layer separation. Affected units include catalog 0400-820-100 with listed lot numbers.
Separation of material layers may occur, causing a potential risk of exposure to contaminants.
Stryker is recalling certain T5 Zipper Toga with Peel-Away Face Shield items due to a risk of contaminant exposure from material layers separating. This could happen during normal use and may require special handling.
The Toga's material layers might separate, allowing contaminants to come into contact with the user. This could happen during normal use, especially if the gear is handled improperly or exposed to moisture.
Healthcare workers using sterile protective gear in medical settings are most at risk. Patients and others exposed to the contaminated gear could also be affected.
Check for the catalog number 0400-820-100 and lot numbers listed: 17061816, 17061836, 17061839, 17061853, 17071921, 17072017, 17102944, 17102948, 17113081, 17113141, 17113194.
Verify the catalog number 0400-820-100 and lot numbers listed in the recall notice.
Material layers may separate, causing potential exposure to contaminants during normal use.
Check for catalog number 0400-820-100 and lot numbers: 17061816, 17061836, 17061839, 17061853, 17071921, 17072017, 17102944, 17102948, 17113081, 17113141, 17113194.
The recall does not specify a stop-use action; check the product details to confirm if it's affected.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1507-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1507-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.