Recall Z-2287-2018— Teleflex Medical Europe Ltd

Name: FDA recall Z-2287-2018
Creator: U.S. Food and Drug Administration
Published: 2018-06-12

Class II · Terminated

Class II FDA medical device recall by Teleflex Medical Europe Ltd, initiated 2018-06-12, terminated 2021-04-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors. Reason: The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized..

Recalling firm: Teleflex Medical Europe Ltd
Classification: Class II
Status: Terminated
Initiated: 2018-06-12
Terminated: 2021-04-02
Firm location: Athlone, Ireland

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.