PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot codes: 19UBB149, b. KIT LB SHUNT, Model NumberDYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567 Model/Catalog Number: a. Model Number DYNJ36725B, b. Model Number DYNJ905860A

Reported: August 3, 2022 Initiated: June 6, 2022 #Z-1471-2022

Product Description

Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot codes: 19UBB149, b. KIT LB SHUNT, Model NumberDYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567 Model/Catalog Number: a. Model Number DYNJ36725B, b. Model Number DYNJ905860A

Reason for Recall

Kits contain leaking bottles of isopropyl alcohol

Details

Units Affected
288 units
Distribution
US Nationwide distribution.
Location
Waukegan, IL

Frequently Asked Questions

What product was recalled?
Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot codes: 19UBB149, b. KIT LB SHUNT, Model NumberDYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567 Model/Catalog Number: a. Model Number DYNJ36725B, b. Model Number DYNJ905860A. Recalled by MEDLINE INDUSTRIES, LP - SPT. Units affected: 288 units.
Why was this product recalled?
Kits contain leaking bottles of isopropyl alcohol
Which agency issued this recall?
This recall was issued by the FDA Devices on August 3, 2022. Severity: Moderate. Recall number: Z-1471-2022.