# FDA recall Z-1430-2023

> **Aesculap Implant Systems LLC** · Class II · device recall initiated 2023-02-23.

## Product

Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and  ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only.  A lid to a container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments.    Note: The CCR basket lid is also distributed with ME764 CCR Basket - Full System

## Reason for recall

Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct  GTIN # is 04046955299607.

## Distribution

US Nationwide distribution in the states of CA, OH, NE, NH, FL, PA, TX.

## Key facts

- **Recall number:** Z-1430-2023
- **Recalling firm:** Aesculap Implant Systems LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-23
- **Report date:** 2023-05-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1430-2023

## Citation

> AI Analytics. FDA recall Z-1430-2023. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1430-2023. Source: US FDA. Licensed CC0.

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