FDA recall record

Hill-Rom Centrella Smart+ Bed, Catalog Number P7900 recall — FDA Z-2246-2020

The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse…

Class IIclassification
Z-2246-2020official record ID
Jun 10, 2020report date

Recall record at a glance

Official recordZ-2246-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHill-Rom, Inc.
Report dateJun 10, 2020
Recall initiation dateApr 30, 2020
Quantity4381 beds
LocationBatesville, IN, United States

Official product description

Centrella Smart+ Bed, Catalog Number P7900

Why the product was recalled

The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse call wall unit.

Distribution information

Domestic distribution nationwide. Foreign distribution 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.

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