Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month shelf life label (should be 36 months). Affected items have specific catalog numbers and lot numbers.
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5 year) shelf life.
Stryker is recalling disposable Spetzler-Malis bipolar forceps that have an incorrect shelf life label. The product should last 36 months but the label shows 54 months. This means the items might be used beyond their safe expiration date.
The product label shows a 54-month shelf life when it should be 36 months. This could mean the items might be used after their safe expiration date, potentially affecting their performance in medical procedures.
Surgical staff and medical professionals who use these disposable forceps for procedures. The risk is low as the hazard is a labeling error, not a safety issue.
Check for the catalog number 6780-200-010 and lot numbers 200525011, 200806012, or 201015015. The product is a disposable Spetzler-Malis bipolar forceps with a 20cm length and 1.0mm bayonet.
Look for the catalog number 6780-200-010 and lot numbers 200525011, 200806012, or 201015015 on the product.
The product label shows a 54-month shelf life when it should be 36 months, which could mean the items are used beyond their safe expiration date.
Check the product label for the catalog number 6780-200-010 and lot numbers 200525011, 200806012, or 201015015. If you have these, contact Stryker for guidance.
No, this is a labeling error that could affect product performance but does not pose a safety risk like injury or fire.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0253-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0253-2024 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.
