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 expiration date on their label. The product should last 36 months but the label shows 54 months. This could lead to using expired products if not noticed.
The product label shows a 54-month shelf life when it should be 36 months. This could cause healthcare workers to use expired instruments, potentially leading to reduced effectiveness or contamination risks.
Healthcare professionals using these surgical instruments are most likely affected. The risk is low as the hazard is a labeling error, not a safety issue.
Check for the catalog number 6780-230-015 and lot numbers 200423023, 200525015, 200806014, or 201015018. The product is a disposable Spetzler-Malis bipolar forceps, 23cm with a 1.5mm bayonet.
Look for the catalog number 6780-230-015 and lot numbers listed in the recall notice.
The product label shows a 54-month shelf life when it should be 36 months, which could lead to using expired instruments.
Check the product label for the catalog number 6780-230-015 and lot numbers 200423023, 200525015, 200806014, or 201015018. If you have the correct items, contact Stryker for guidance.
The recall is for a labeling error, not a safety hazard. The risk is low as the product is not expected to cause injury if used properly.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0257-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0257-2024 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.
