FDA recall record

Invacare Assist Bed Rail - 6632 recall — FDA Z-2218-2017

A typographical error was noted within the user manual for the 6632 Assist Bed Rail which could result in the Assist Bed Rails being installed incorrectly.

Class IIclassification
Z-2218-2017official record ID
Jun 7, 2017report date

Recall record at a glance

Official recordZ-2218-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmInvacare Corporation
Report dateJun 7, 2017
Recall initiation dateApr 25, 2017
Quantity5,020 Units
LocationElyria, OH, United States

Official product description

Assist Bed Rail - 6632

Why the product was recalled

A typographical error was noted within the user manual for the 6632 Assist Bed Rail which could result in the Assist Bed Rails being installed incorrectly.

Distribution information

Product was shipped to all US states plus the District of Columbia. Product was also shipped to Canada and Australia.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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