Kimberly-Clark Corporation: Medical Device Recalls in 2013

According to to data from the FDA, there were 2 medical device recalls made by Kimberly-Clark Corporation in 2013. See the details of the recalls below.

You can see similar recalls for other firms.

• KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose another medical device that is to be sterilized by a health care provider.
• Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs