Intrinsic Therapeutics recalls Barricaid Annual Closure Device BAR-A8-8MM due to incorrect catalog number on patient stickers. The label shows BAR-A8-10MM instead of BAR-A8-8MM. This may cause confusion but does not pose a safety risk.
The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.
Intrinsic Therapeutics is recalling Barricaid Annual Closure Devices (BAR-A8-8MM) because the catalog number on the patient sticker is incorrect. The label shows BAR-A8-10MM instead of BAR-A8-8MM. This error could lead to confusion about the product but does not cause safety risks.
The catalog number on the patient sticker is listed as BAR-A8-10MM instead of BAR-A8-8MM. This mismatch could cause confusion about the product's specifications but does not affect safety or functionality.
Patients who own the Barricaid ACD BAR-A8-8MM with the incorrect catalog number on the patient sticker. Those most at risk are individuals using the device for spinal conditions.
Check the patient sticker on the inner container (box) for the catalog number. It should read BAR-A8-8MM, not BAR-A8-10MM.
Look for the catalog number on the patient sticker; it should be BAR-A8-8MM.
The catalog number on the patient sticker is incorrect, showing BAR-A8-10MM instead of BAR-A8-8MM.
No, this error does not pose a safety risk. It only causes confusion about the product's specifications.
Check the catalog number on the patient sticker. If it shows BAR-A8-10MM, contact Intrinsic Therapeutics for clarification.
We’ve drafted a message you can send Intrinsic Therapeutics to request your refund or repair — edit it as you like.
Subject: Recall Z-2798-2020 — Intrinsic Therapeutics Intrinsic Therapeutics Hello, I own a Intrinsic Therapeutics that is covered by recall Z-2798-2020 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.
