Synthes recalls 690.379 Graphic Case F/6.5mm Cannulated Screw Set due to screws measuring 5. 41mm shorter than actual length. This could lead to improper surgical fixation. Affected units sold in the US.
Affected screw gauges incorrectly measure screws 5.41mm shorter than the actual overall screw length.
Synthes is recalling a specific surgical screw set because the screws are incorrectly measured as 5.41mm shorter than their actual length. This risk could cause improper surgical fixation if used in procedures requiring precise screw length.
The screws are labeled as 6.5mm but actually measure 5.41mm shorter than the intended length. This discrepancy could cause the screws to be too short for proper surgical fixation, potentially leading to complications like loosening or failure of the implant.
Surgical professionals and hospitals that purchased the recalled screw set (part no. 690.379) in the US. Patients using these screws for surgery are at risk if the incorrect measurement leads to improper fixation.
Check for the part number 690.379 on the Graphic Case F/6.5mm Cannulated Screw Set packaging. The recall was issued for products sold in the US with the code FL00860.
Verify the part number on the packaging to confirm if it matches 690.379.
The recall applies to the screw set used in surgery. If you have the recalled part number, your surgeon may need to check if the screws were used correctly.
Check the packaging for part number 690.379 on the Graphic Case F/6.5mm Cannulated Screw Set. The recall was issued for products sold in the US with code FL00860.
The recall does not specify a remedy, so you should contact Synthes directly to discuss next steps.
We’ve drafted a message you can send Synthes to request your refund or repair — edit it as you like.
Subject: Recall Z-2246-2018 — Synthes Synthes Hello, I own a Synthes that is covered by recall Z-2246-2018 from Synthes. 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.
