Intrinsic Therapeutics recalls Barricaid Annular Closure Impactor units with missing welds. Affected units have specific lot numbers and part numbers. Consumers should check their product details to determine if they are affected.
At least two units have been found to be missing a weld.
Intrinsic Therapeutics is recalling Barricaid Annular Closure Impactor devices that may have a missing weld. This defect could lead to improper function or failure of the device, though the recall does not specify serious injury risks.
The device may have a missing weld, which could cause improper function or failure. However, the recall does not specify that this defect leads to serious injury or death in normal use.
Users of the Barricaid Annular Closure Impactor device with specific lot numbers and part numbers are affected. The risk is low as the recall does not indicate serious injury potential.
Check for the part number 400906-A and lot numbers 10282203, 06152307, 08292301, or 10112307 on the device. The product is sold under the reference code BAR-IMPACTOR.
Look for the part number 400906-A and lot numbers 10282203, 06152307, 08292301, or 10112307 on the device.
The recall states that at least two units have a missing weld, but it does not specify that this causes serious injury or death in normal use.
Check for the part number 400906-A and lot numbers 10282203, 06152307, 08292301, or 10112307 on the device.
The recall does not provide a specific remedy, so no action is required beyond checking if your product matches the affected details.
We’ve drafted a message you can send Intrinsic Therapeutics to request your refund or repair — edit it as you like.
Subject: Recall Z-2688-2024 — Intrinsic Therapeutics Intrinsic Therapeutics Hello, I own a Intrinsic Therapeutics that is covered by recall Z-2688-2024 from Intrinsic Therapeutics. 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.
