RecallRadar

FDA Device recall Z-3022-2026

Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U

On 2026-09-02 the FDA classified a Class II recall of Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U by Medline Industries, citing kits contain a potentially contaminated component which were recalled by the manufacturer.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3022-2026
ClassificationClass II
Statusongoing
Initiated2026-07-10
Published2026-09-02
Last updated2026-09-13 11:58 UTC
CompanyMedline Industries
DistributionUS

Product

Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY, Medline Kit SKU DYNJ903479L; 4) LAPAROSCOPY, Medline Kit SKU DYNJ903479M.

Reason

Kits contain a potentially contaminated component which were recalled by the manufacturer

Identifiers

code_info
Medline Kit SKU CDS982040U, UDI/DI 10198459385421 (each) 40198459385422 (case), Lot Number 26AMC355; Medline Kit SKU D…Medline Kit SKU CDS982040U, UDI/DI 10198459385421 (each) 40198459385422 (case), Lot Number 26AMC355; Medline Kit SKU DYNJ89608, UDI/DI 10198459279324 (each) 40198459279325 (case), Lot Number 25JBR465; Medline Kit SKU DYNJ903479L, UDI/DI 10198459255250 (each) 40198459255251 (case), Lot Number 25LMB480; Medline Kit SKU DYNJ903479M, UDI/DI 10198459790591 (each) 40198459790592 (case), Lot Number 26FMB173.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3022-2026%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.