FDA Recall
Terminated
Non-Rebreather Oxygen Mask, Pediatric with Tubing, Product Code 86-3226E, Product Code PMD06009, Product Code PMD06106
Recall: Z-2243-2017
·
Initiated May 10, 2017
Recall
- Recall Number
- Z-2243-2017
- Event Number
- 77282
- Firm
- ConvaTec, Inc
- FEI Number
- 3011987967
- Product Code
- BYG
- Status
- Terminated
- Root Cause
- Process control
- Initiated
- May 10, 2017
- Posted
- May 24, 2017
- Terminated
- August 27, 2021
- Address
- 7900 Triad Center Dr, Ste 400, Greensboro, NC, 27409-9076
Description
Non-Rebreather Oxygen Mask, Pediatric with Tubing, Product Code 86-3226E, Product Code PMD06009, Product Code PMD06106
Action
Recall Letters were sent to consignees on May 10, 2017. The letter requested that they immediately stop distribution and quarantine all affected lots. The letter also requested a sub-recall if the product had been further distributed. Also attached to the letter is a Recall Response Form to be returned.
Distribution
CA, CT, FL, GA, IL, MO, NJ, NY, NC, OH, PA, RI, VA , Puerto Rico, Australia, Belgium, Canada, Columbia, Czech, Denmark, Finland, France, Germany, Greece, Israel, Italy, Japan, Jordan, Malaysia, Malta, Netherlands, Norway, Rwanda, Saudi Arabia, Sweden, Switzerland, United Kingdom, and Vietnam