ZPLP(Zimmer Periarticular Locking Plate System) Distal recall
ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated for temporary internal…
Why was ZPLP(Zimmer Periarticular Locking Plate System) Distal recalled?
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI: (01)00889024088573(17)290510(10)64370380 (01)00889024088573(17)290517(10)64370382 (01)00889024088573(17)290607(10)64423329 (01)00889024088573(17)290811(10)64475643 (01)00889024088573(17)300225(10)64661551 (01)00889024088573(17)300307(10)64661552 (01)00889024088573(17)300511(10)64745739 (01)00889024088573(17)300506(10)64745742 (01)00889024088573(17)300506(10)64745744 (01)00889024088573(17)300506(10)64745745 (01)00889024088573(17)321209(10)65635924 (01)00889024088573(17)321207(10)65645147 (01)00889024088573(17)330215(10)65755766 (01)00889024088573(17)330430(10)65997131 (01)00889024088573(17)330428(10)65997134 (01)00889024088573(17)330430(10)66023658 (01)00889024088573(17)330730(10)66166098 (01)00889024088573(17)330811(10)66201200 (01)00889024088573(17)330822(10)66233083 (01)00889024088573(17)330822(10)66233084 Lot Numbers: 64370380 64370382 64423329 64475643 64661551 64661552 64745739 64745742 64745744 64745745 65635924 65645147 65755766 65997131 65997134 66023658 66166098 66201200 66233083 66233084
- Product
- ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated for temporary internal…
- Recalling firm
- Zimmer, Inc.
- Distribution
- Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.
- Recall date
- May 8, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)