Z-2922-2020 Class II Terminated
FDA device recall Z-2922-2020 was initiated by TELEFLEX MEDICAL INC on August 7, 2020 and is designated Class II. Reason for recall: Potential sterility issue The recall status is terminated (terminated January 14, 2023). Affected quantity: 700 eaches.
Recall Details
- Product Type
- Devices
- Report Date
- September 9, 2020
- Initiation Date
- August 7, 2020
- Termination Date
- January 14, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 700 eaches
Product Description
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. The thoracic catheter is indicated for use less than 30 days.
Reason for Recall
Potential sterility issue
Distribution Pattern
US Distribution of states to: AR AZ CA CO FL GA IA IL IN LA MI MN MS NC NH NV NY OH OK OR PA SD TN TX VA WA WI
Code Information
74K1900074 74K1901335 74L1901435 74M1900809