FDA recall record

Integra Universal Flexible Arm part number REF 1362275 recall — FDA Z-0906-2022

Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.

Class IIclassification
Z-0906-2022official record ID
Apr 20, 2022report date

Recall record at a glance

Official recordZ-0906-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmIntegra LifeSciences Corp.
Report dateApr 20, 2022
Recall initiation dateFeb 28, 2022
Quantity54
LocationPrinceton, NJ, United States

Official product description

Integra Universal Flexible Arm part number REF 1362275

Why the product was recalled

Excess force used to tighten the Universal Flexible Arm can cause the internal cable to break at the tip, resulting in an unusable condition.

Distribution information

US Nationwide Distribution: AL, AZ, FL, GA, IL, MA, MD, NY, OH, OR, PA, TX

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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