Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month expiration date label (should be 36 months). Affected units may expire sooner than intended.
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 label showing 54 months instead of the actual 36-month shelf life. This means the products could expire sooner than intended, potentially leading to ineffective use in medical procedures.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. This means the instruments could become ineffective or unsafe for use after the intended 36-month period, potentially affecting medical procedures.
Medical professionals using these disposable surgical instruments are likely affected. Patients using the instruments during procedures may be at risk if the instruments become ineffective due to expiration.
Check for disposable Spetzler-Malis bipolar forceps with catalog number 6760-180-005, lot number 200507002, or the GTIN 7613327300192. The product label shows a 54-month expiration date instead of 36 months.
Verify the product label shows a 54-month expiration date instead of the correct 36-month shelf life.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months, which could lead to ineffective use of the instruments.
Check for disposable Spetzler-Malis bipolar forceps with catalog number 6760-180-005, lot number 200507002, or GTIN 7613327300192. The label shows a 54-month expiration date instead of 36 months.
The recall does not specify a remedy, so no action is required beyond checking the expiration date label.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0239-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0239-2024 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.
