Recall Z-0039-2018— Teleflex Medical
Class II · Completed
Class II FDA medical device recall by Teleflex Medical, initiated 2014-09-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.. Reason: The knife handles slot depth is out of specification, so blades may not fit on the handles properly..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Completed
- Initiated
- 2014-09-26
- Firm location
- Research Triangle Park, NC, United States
Product description
Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.
Reason for recall
The knife handles slot depth is out of specification, so blades may not fit on the handles properly.
Data sourced from openFDA. This site is unofficial and independent of the FDA.