PPS RingLoc+ Acetabular Shell recall
PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended to replace the natural…
Why was PPS RingLoc+ Acetabular Shell recalled?
Device was distributed with the etching missing from the product.
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?
Model No. 11-116062, Lot No. 374670, UDI No. (01) 0 0880304 59316 9 (17) 270513 (10) 374670
- Product
- PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended to replace the natural…
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 15 units
- Distribution
- Distributed domestically to MI, MN, ND.
- Recall date
- January 10, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)