ZPLP (Zimmer Periarticular Locking Plate System) Distal recall
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 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)00889024088498(17)321205(10)65620069 (01)00889024088498(17)321205(10)65635922 (01)00889024088498(17)321205(10)65635923 (01)00889024088498(17)330111(10)65674071 (01)00889024088498(17)330115(10)65674072 (01)00889024088498(17)330428(10)66010704 (01)00889024088498(17)330730(10)66166096 (01)00889024088498(17)330822(10)66216633 Lot Numbers: 65620069 65635922 65635923 65674071 65674072 66010704 66166096 66216633
- Product
- ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 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)