ZPLP (Zimmer Periarticular Locking Plate System) Distal recall
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 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)00889024088580(17)300112(10)64568169 (01)00889024088580(17)300307(10)64697763 (01)00889024088580(17)300225(10)64697764 (01)00889024088580(17)330215(10)65755769 (01)00889024088580(17)330218(10)65782566 (01)00889024088580(17)330211(10)65782567 (01)00889024088580(17)331208(10)66233085 Lot Numbers: 64568169 64697763 64697764 65755769 65782566 65782567 66233085
- Product
- ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 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)