FDA recall record

Defibtech RMU-2000 Automated Chest Compression Device recall — FDA Z-2543-2024

Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could…

Class Iclassification
Z-2543-2024official record ID
Aug 21, 2024report date

Recall record at a glance

Official recordZ-2543-2024
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmDefibtech, LLC
Report dateAug 21, 2024
Recall initiation dateJul 12, 2024
Quantity174 US, 37 OUS
LocationGuilford, CT, United States

Official product description

RMU-2000 Automated Chest Compression Device

Why the product was recalled

Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death.

Distribution information

Domestic distribution to CT, FL, NJ, SC, TN. Foreign distribution to Japan

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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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