FDAClass IISeptember 9, 2015

EXTREMITY ARM PACK 4/CS HOSP. DR. CENTER Used by recall

EXTREMITY ARM PACK 4/CS HOSP. DR. CENTER Used by medical staff to perform surgical procedures and patient care procedures such as wound healing…

Why was EXTREMITY ARM PACK 4/CS HOSP. DR. CENTER Used by 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:9002438 Lots: 140915317 exp. 2/29/16 140714246 exp. 11/30/15 141216303 exp. 12/31/15 150116527 exp. 1/31/16 150317827 exp. 5/31/16 150418359 exp. 5/31/16 150518812 exp. 5/31/16

Product
EXTREMITY ARM PACK 4/CS HOSP. DR. CENTER Used by medical staff to perform surgical procedures and patient care procedures such as wound healing…
Recalling firm
Customed, Inc
Quantity
148
Distribution
Distributed Only in Puerto Rico.
Recall date
September 9, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls