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Arise 1000 EX AREXLAL-CURecalls & reported problems

Joerns Healthcare, LLC · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Oct 31, 2025Class IIOpen, Classified

    Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.

    Z-0919-2026 · Root cause: Release of Material/Component prior to receiving test results · Recall details · FDA record ↗

Other Mattress, Air Flotation, Alternating Pressure devices

All Mattress, Air Flotation, Alternating Pressure devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page