RecallRadar

FDA Device recall Z-0172-2027

Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D

On 2026-10-21 the FDA classified a Class II recall of Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D by Medline Industries, citing medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking duri….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0172-2027
ClassificationClass II
Statusongoing
Initiated2026-09-02
Published2026-10-21
Last updated2026-10-27 05:30 UTC
CompanyMedline Industries
DistributionUS

Product

Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D

Reason

Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Identifiers

code_infoUDI/DI 10195327005412 (each) 40195327005413 (case), Lot number 23JMA378

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-27 05:30 UTC. Current status: ongoing.

Other recalls by Medline Industries

All Medline Industries recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0172-2027%22

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