Recall Z-1951-2014— Medical Action Industries Inc
Class II · Terminated
Class II FDA medical device recall by Medical Action Industries Inc, initiated 2014-06-12, terminated 2015-02-03. FDA's recall record names no specific 510(k) clearance for this event. Product: Laceration/Suture Removal, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.. Reason: Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits..
- Recalling firm
- Medical Action Industries Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-06-12
- Terminated
- 2015-02-03
- Firm location
- Arden, NC, United States
Product description
Laceration/Suture Removal, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.
Reason for recall
Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Data sourced from openFDA. This site is unofficial and independent of the FDA.