FDA recall record

ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800 recall — FDA Z-0802-2019

Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This,…

Class IIclassification
Z-0802-2019official record ID
Feb 13, 2019report date

Recall record at a glance

Official recordZ-0802-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmArjohuntleigh Magog
Report dateFeb 13, 2019
Recall initiation dateDec 19, 2018
Quantity231 units
LocationMagog, Quebec, Canada

Official product description

ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800

Why the product was recalled

Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event.

Distribution information

US, Saudi Arabia, and Kuwait

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: Visit.

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.

Related recall records

Other records from the same recalling company are shown first when available.