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 dates.
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, which could lead to using expired medical tools.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. Using expired medical tools could potentially lead to reduced effectiveness or safety issues during procedures.
Medical professionals who use these disposable surgical instruments are likely affected. Patients using the recalled instruments during procedures may be at slightly higher risk if the tools are expired.
Check for the catalog number 6780-200-005 on the product label. Affected items were sold with lot numbers 201008016, 201015014, 201029008, or 201210016.
Look for the catalog number 6780-200-005 and lot numbers 201008016, 201015014, 201029008, or 201210016.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months.
Check the product label for the catalog number 6780-200-005 and lot numbers 201008016, 201015014, 201029008, or 201210016. If you have these, contact Stryker for guidance.
The recall is for an incorrect expiration date label, not a safety hazard. Using expired tools could reduce effectiveness but does not pose a direct injury risk.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0252-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0252-2024 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.
