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Aesculap Implant Systems LLC recalls Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR) Basket Full System -
Recalled May 3, 2023 · FDA recall Z-1430-2023 · Aesculap Implant Systems
Hazard
Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607. · FDA Class II
Units
ME754: 3 units; ME764: 22 units
Sold at
US Nationwide distribution in the states of CA, OH, NE, NH, FL, PA, TX.
Description
Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607.
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
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →