Z-2531-2018 Class II Terminated
FDA device recall Z-2531-2018 was initiated by Brewer Company, LLC on March 29, 2018 and is designated Class II. Reason for recall: One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table. The recall status is terminated (terminated August 29, 2019). Affected quantity: 7 devices.
Recall Details
- Product Type
- Devices
- Report Date
- August 1, 2018
- Initiation Date
- March 29, 2018
- Termination Date
- August 29, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7 devices
Product Description
Access Hi-Low Exam Tables, Model 6501-XX
Reason for Recall
One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table.
Distribution Pattern
Devices distributed in WI, TX, MN and IL.
Code Information
Model 6501-XX, Lot/Serial No. HL018786, HL018787, HL018788, HL018789, HL018790, HL018791, HL018797, HL018805