# FDA recall Z-2651-2023

> **Covidien** · Class II · device recall initiated 2023-08-22.

## Product

Puritan Bennett Cuff Pressure Manager, REF: 180-03

## Reason for recall

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.

## Distribution

US: AL, NJ, MA, MI, NY, NC, CO, TX, FL, KY, UT, CA, AZ, KS, IL, TN. OUS: El Salvador, Sweden, Canary Islands

## Key facts

- **Recall number:** Z-2651-2023
- **Recalling firm:** Covidien
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-22
- **Report date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Boulder, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2651-2023

## Citation

> AI Analytics. FDA recall Z-2651-2023. Retrieved 2026-08-20 from https://api.ai-analytics.org/recall/Z-2651-2023. Source: US FDA. Licensed CC0.

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