# FDA recall Z-2155-2018

> **Sun Med, LLC** · Class II · device recall initiated 2018-05-24.

## Product

MEDLINE ADULT MANUAL RESUSCITATOR WITH LARGE ADULT MASK, TUBE RESERVOIR, FILTER AND 7 FT. OXYGEN TUBING, REF CPRM1126FL

## Reason for recall

There is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use.  This may impact air delivery to the patient.

## Distribution

IL & OH distributors

## Key facts

- **Recall number:** Z-2155-2018
- **Recalling firm:** Sun Med, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-24
- **Report date:** 2018-06-20
- **Termination date:** 2020-05-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grand Rapids, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2155-2018

## Citation

> AI Analytics. FDA recall Z-2155-2018. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2155-2018. Source: US FDA. Licensed CC0.

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