PERI GYN PACK CS/6 Used by medical staff to perform recall
PERI GYN PACK CS/6 Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate…
Why was PERI GYN PACK CS/6 Used by medical staff to perform 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:9001061 Lots: 141015757 exp. 10/31/15 141216313 exp. 12/31/15 150116727 exp. 1/31/16 150116973 exp. 1/31/16 150116980 exp. 1/31/16 150418280 exp. 4/30/16 150518620 exp. 5/31/16 150519110 exp. 5/31/16
- Product
- PERI GYN PACK CS/6 Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate…
- Recalling firm
- Customed, Inc
- Quantity
- 228 packs
- Distribution
- Distributed Only in Puerto Rico.
- Recall date
- September 9, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)