FDAClass IIJanuary 25, 2017

Active Articulation ArComXL Polyethylene Bearings recall

Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152

Why was Active Articulation ArComXL Polyethylene Bearings recalled?

Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery.

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

Item XL-200152 Lot 339260 UDI (01)00880304491366(17)210713(10)339260

Product
Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152
Recalling firm
Zimmer Biomet, Inc.
Quantity
19
Distribution
USA (nationwide) and Internationally to ARGENTINA
Recall date
January 25, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls