FDA Device recall Z-1957-2014
Laceration Kit: W/Needles, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC
- FDA Device
- Class II
- terminated
- Published 2014-07-09
On 2014-07-09 the FDA classified a Class II recall of Laceration Kit: W/Needles, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC by Medical Action Industries, citing some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1957-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-12 |
| Published | 2014-07-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medical Action Industries |
| Distribution | AR, AZ, FL, GA, IA, IL, KY, MA, MN, NC, NY, OH, TN, TX, VA |
Product
Laceration Kit: W/Needles, 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.
Identifiers
| code_info | Model number: 68718, Lot number: 187198, Exp. Date: 12/1/2016. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1957-2014%22
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