AcuMatch A-Series Connexion GXL Enhanced Polyethylene recall
AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.
Why was AcuMatch A-Series Connexion GXL Enhanced Polyethylene recalled?
Products were labeled with incorrect Global Trade Item Numbers. The GTIN on the label identifies the devices as another.
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?
Serial No. 4507932-4507943; Catalog No. 138-36-29; UDI: 10885862024831
- Product
- AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.
- Recalling firm
- Exactech, Inc.
- Quantity
- 12 devices
- Distribution
- AZ, CA, CO, FL, IL, KS, MD, NJ, NY, OH, OK, TN, & VA; Germany, Italy, Japan, Spain, & Switzerland.
- Recall date
- January 25, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)