Official recall record
Puritan Bennett Cuff Pressure Manager, REF: 180-03
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-08-22
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 10884521782495
- Brand on record
- Covidien
- Product category
- Medical Device
What the authority reported
Inadequate internal fixation of the power inlet port to the cuff pressure manager device causes the external power inlet to became dislodged within the device housing after several uses, which prevents the device from being charged, and could lead to treatment delay.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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All 13 official recall notices naming Covidien LP on this site →
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