Stryker recalls Infinity Alignment Frame Distal Sub-Assembly (Catalog #33600020) due to pin sleeve holes being too narrow, preventing proper pin placement. Affected units include specific lot numbers.
The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.
Stryker is recalling a specific part for surgical alignment frames because the pin sleeve holes are too narrow. This prevents proper pin placement, which could lead to incorrect surgical positioning.
The pin sleeve holes are too narrow, so the pin sleeves cannot pass through them. This prevents correct pin placement through the pin holes, potentially causing incorrect surgical alignment.
Surgical professionals using the Infinity Alignment Frame Distal Sub-Assembly for procedures. The risk is low as the issue affects only specific parts and not the entire product line.
Check for the catalog number 33600020 on the product. Affected units have lot numbers 2656815 or 2762126 and UDI-DI 00889797003926.
Verify the catalog number and lot numbers to confirm if your item is affected.
The pin sleeve holes are too narrow, preventing proper pin placement through the pin holes.
Lot numbers 2656815 and 2762126.
Look for catalog number 33600020 and lot numbers 2656815 or 2762126.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2105-2023 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2105-2023 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.
