Z-2287-2018 Class II Terminated
FDA device recall Z-2287-2018 was initiated by Teleflex Medical Europe Ltd on June 12, 2018 and is designated Class II. Reason for recall: The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized. The recall status is terminated (terminated April 2, 2021). Affected quantity: 573 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 4, 2018
- Initiation Date
- June 12, 2018
- Termination Date
- April 2, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 573 units
Product Description
Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
Reason for Recall
The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized.
Distribution Pattern
Worldwide Distribution - US Nationwide and the countries of Canada, India
Code Information
Lot Numbers: F7, G7