Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month expiration date 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 shows a 54-month shelf life but should only be used within 36 months. This could lead to potential quality issues if used beyond the correct shelf life.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. Using the instruments beyond this period could lead to potential quality issues, though serious injury is not expected.
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 beyond the correct shelf life.
Check for the product name 'Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 1.5MM TIP' with catalog number 6770-200-015. Lot numbers 200731010 and 201008012 are also associated with this recall.
Verify the product's expiration date against the actual shelf life of 36 months from the manufacturing date.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months.
The recall does not specify a remedy, so check the expiration date against the 36-month shelf life.
Look for the product name 'Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 1.5MM TIP' with catalog number 6770-200-015 and lot numbers 200731010 or 201008012.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0249-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0249-2024 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.
