FDA Device recall Z-1602-2025

Refer to RES

FDA Device
Class II
ongoing
Published 2025-04-23

On 2025-04-23 the FDA classified a Class II recall of Refer to RES by Medline Industries Northfield, citing there is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1602-2025
Classification	Class II
Status	ongoing
Initiated	2025-03-03
Published	2025-04-23
Last updated	2026-09-13 11:57 UTC
Company	Medline Industries Northfield
Distribution	US

Product

Refer to RES

Reason

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Identifiers

code_info	1) DYNJHTLD02A, UDI-DI: 10193489303360(each), 40193489303361(case), Lot Number: 24IBE784; 2) DYNJ50017B, UDI-DI: 108899… 1) DYNJHTLD02A, UDI-DI: 10193489303360(each), 40193489303361(case), Lot Number: 24IBE784; 2) DYNJ50017B, UDI-DI: 10889942851126(each), 40889942851127(case), Lot Number: 24IBE809; 3) DYNJ68242C, UDI-DI: 10198459091568(each), 40198459091569(case), Lot Number: 24IBF050; 4) SYNJ10001B, UDI-DI: 10195327067977(each), 40195327067978(case), Lot Number: 24IBF241; 5) DYNJ42691, UDI-DI: 10888277003507(each), 40888277003508(case), Lot Number: 24IBF320; 6) DYNJ43775C, UDI-DI: 10889942763191(each), 40889942763192(case), Lot Number: 24IBF620; 7) DYNJ54078A, UDI-DI: 10193489528633(each), 40193489528634(case), Lot Number: 24IBF640; 8) DYNJ39493B, UDI-DI: 10889942669998(each), 40889942669999(case), Lot Number: 24IBG032; 9) DYNJ0101397O, UDI-DI: 10195327661663(each), 40195327661664(case), Lot Number: 24IBG201; 10) DYNJ28408J, UDI-DI: 10195327279684(each), 40195327279685(case), Lot Number: 24IBG536; 11) DYNJ45997C, UDI-DI: 10889942684366(each), 40889942684367(case), Lot Number: 24IBG574; 12) DYNJ17504G, U

code_info

1) DYNJHTLD02A, UDI-DI: 10193489303360(each), 40193489303361(case), Lot Number: 24IBE784; 2) DYNJ50017B, UDI-DI: 108899…

1) DYNJHTLD02A, UDI-DI: 10193489303360(each), 40193489303361(case), Lot Number: 24IBE784; 2) DYNJ50017B, UDI-DI: 10889942851126(each), 40889942851127(case), Lot Number: 24IBE809; 3) DYNJ68242C, UDI-DI: 10198459091568(each), 40198459091569(case), Lot Number: 24IBF050; 4) SYNJ10001B, UDI-DI: 10195327067977(each), 40195327067978(case), Lot Number: 24IBF241; 5) DYNJ42691, UDI-DI: 10888277003507(each), 40888277003508(case), Lot Number: 24IBF320; 6) DYNJ43775C, UDI-DI: 10889942763191(each), 40889942763192(case), Lot Number: 24IBF620; 7) DYNJ54078A, UDI-DI: 10193489528633(each), 40193489528634(case), Lot Number: 24IBF640; 8) DYNJ39493B, UDI-DI: 10889942669998(each), 40889942669999(case), Lot Number: 24IBG032; 9) DYNJ0101397O, UDI-DI: 10195327661663(each), 40195327661664(case), Lot Number: 24IBG201; 10) DYNJ28408J, UDI-DI: 10195327279684(each), 40195327279685(case), Lot Number: 24IBG536; 11) DYNJ45997C, UDI-DI: 10889942684366(each), 40889942684367(case), Lot Number: 24IBG574; 12) DYNJ17504G, U

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1602-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.