Integra recalls Universal Flexible Arm part REF 1362275 due to cable breakage from excessive tightening. Affected units include specific lots and UDI numbers. No remedy provided in official notice.
Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.
Integra is recalling a Universal Flexible Arm part because tightening it too hard can break the internal cable, making it unusable. This affects specific production lots and unique identifiers.
Excessive force when tightening the Universal Flexible Arm can cause the internal cable to break at the tip. This results in the arm becoming unusable but does not typically cause injury or damage to the user.
Users of the Integra Universal Flexible Arm part number REF 1362275 with specific production lots (AC2109, AC2103, etc.) and UDI number 10381780074670 are affected. The risk is low as the hazard only causes an unusable condition, not injury.
Check if your Universal Flexible Arm has part number REF 1362275 and UDI number 10381780074670. Affected units include production lots AC2109, AC2103, AC2106, AC2110, AC2101, AC2008, and AC2009.
Verify your Universal Flexible Arm has part number REF 1362275 and UDI number 10381780074670.
The official recall notice does not provide a remedy.
Check for part number REF 1362275 and UDI number 10381780074670. Affected units include production lots AC2109, AC2103, AC2106, AC2110, AC2101, AC2008, and AC2009.
The recall notice does not specify any action steps beyond checking product details.
We’ve drafted a message you can send Integra to request your refund or repair — edit it as you like.
Subject: Recall Z-0906-2022 — Integra Integra Hello, I own a Integra that is covered by recall Z-0906-2022 from Integra. 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.
