RecallDepth

IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.

Company
Medical Action Industries Inc
Recall Initiated
January 15, 2024
Posted
March 28, 2024
Recall Number
Z-1394-2024
Quantity
206,200 kits
Firm Location
Arden, NC

Reason for Recall

The kits contain saline flush syringes which were recalled by the supplier.

Distribution

US Nationwide distribution in the states of MN and ND. There as no foreign/military/government distribution.

Lot / Code Info

Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, and 313961;UDI-DI 10809160020388.

Root Cause

Under Investigation by firm

Action Taken

The recalling firm issued letters via email on 1/15/2024 explaining the details of the event and the actions to take. The consignee is to immediately discontinue use of all recalled Aquastat Prefilled Saline Flush 3mL & 5mL fill in 12mL Syringes contained in the kits. If the consignee has distributed kits containing these syringes, they are to notify their customers by including a copy of the recall letter. A warning label template was enclosed for the consignee to print which can be affixed on all affected kits in inventory. The warning label should be applied to each affected convenience kit and product case in a prominently visible location to the end user. The location of the warning label should not cover any other critical product information found on the existing product labeling. The Recall Response Form was to be completed and returned as soon as possible.

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