AIRCAST 3011-PLRecalls & reported problems
Djo, LLC · VF-PL STERILE CUFF PKG · Class 2
All models of AIRCAST (7)
Data updated Oct 16, 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 16, 2026.
Recalls naming this device
- Jan 17, 2019Open, Classified
The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
Z-1985-2019 · Root cause: Environmental control · Recall details · FDA record ↗
Other SLEEVE, LIMB, COMPRESSIBLE devices
- Kendall 84021Cardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE2 recalls0 reports
- Kendall SCD 29525Cardinal Health, Inc. · Sleeve, Limb, Compressible56 reports
- RAW MATERIAL 30MDjo, LLC · SLEEVE, LIMB, COMPRESSIBLE52 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall 84021BCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall 84021PCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall SCD 295251Cardinal Health, Inc. · Sleeve, Limb, Compressible24 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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