Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month expiration label. Products should be used within 36 months of manufacture to avoid potential quality issues.
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 with an incorrect expiration date label. The product label shows a 54-month shelf life, but the actual shelf life is only 36 months. This could lead to potential quality issues if used beyond the correct expiration date.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. Using the instruments beyond this date could lead to potential quality issues, such as reduced performance or safety concerns in medical procedures.
Medical professionals who use these disposable surgical instruments are likely affected. Patients and healthcare facilities using the recalled product may be at risk if the instruments are used after the expiration date.
Check for the product name 'Disposable Spetzler-Malis Bipolar forceps, 20CM SM DISP BAYONET 0.5MM TIP' with catalog number 6760-200-005. Lot numbers starting with 201105002 are affected.
Verify the expiration date on the product label to ensure it does not exceed 36 months from the manufacturing date.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. This could lead to potential quality issues if used beyond the expiration date.
Check the expiration date on the product label. If the product is past the 36-month shelf life, it should not be used.
Look for the product name 'Disposable Spetzler-Malis Bipolar forceps, 20CM SM DISP BAYONET 0.5MM TIP' with catalog number 6760-200-005 and lot numbers starting with 201105002.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0241-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0241-2024 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.
