# FDA recall Z-1283-2023

> **DeRoyal Industries Inc** · Class II · device recall initiated 2023-02-09.

## Product

DeRoyal SafeLiner Suction Canister, 1000cc, REF PHESL-1000B

## Reason for recall

The reason for the voluntary recall is due to shrinkage of the canister lid. This shrinkage causes the lid not to contact the outer shell to create a seal and thus, it does not create and hold vacuum.

## Distribution

US Nationwide distribution in the states of Arizona, Texas, Virginia, Pennsylvania, California, Missouri, North Carolina, Illinois, Indiana, Ohio, Arkansas.

## Key facts

- **Recall number:** Z-1283-2023
- **Recalling firm:** DeRoyal Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-09
- **Report date:** 2023-03-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Powell, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1283-2023

## Citation

> AI Analytics. FDA recall Z-1283-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1283-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
