Medical Action Industries, Inc. IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Brand
Medical Action Industries, Inc.
Lot Codes / Batch Numbers
Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, and 313961, UDI-DI 10809160020388.
Products Sold
Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, and 313961;UDI-DI 10809160020388.
Medical Action Industries, Inc. is recalling IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile. due to The kits contain saline flush syringes which were recalled by the supplier.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The kits contain saline flush syringes which were recalled by the supplier.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026