KNEE ARTHROSCOPY PK 4/CS Used by medical staff to recall
KNEE ARTHROSCOPY PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals…
Why was KNEE ARTHROSCOPY PK 4/CS Used by medical staff to recalled?
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
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?
Code:9002123 Lots: 141015700 exp. 2/28/16 141216296 exp. 12/31/15 150116519 exp. 1/31/16 150217384 exp. 2/28/16 150317796 exp. 3/31/16 150318119 exp. 4/30/16 150318120 exp. 5/31/16 150418346 exp. 5/31/16 150619248 exp. 6/30/16
- Product
- KNEE ARTHROSCOPY PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals…
- Recalling firm
- Customed, Inc
- Quantity
- 188
- Distribution
- Distributed Only in Puerto Rico.
- Recall date
- September 9, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)