Data Foundry

Medical device recalls 2026

Medline convenience kits labeled as: 1) LAVH — Class II medical device recall Z-3027-2026

Ongoing recall by Medline Industries, LP, reported 2026-09-02, distributed nationwide. Kits contain a potentially contaminated component which were recalled by the manufacturer

Recall numberZ-3027-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-07-10
Classified2026-08-26
Reported by FDA2026-09-02
DistributedNationwide (US)
Quantity169 kits
UPC / GTIN / UDI-DI10195327306793, 10195327306830, 10198459293207, 10198459385827, 10198459794285, 40195327306794, 40195327306831, 40198459293208, 40198459385828, 40198459794286
Lot numbers25JBK543, 25KBP729, 25LBR956, 26DMB880, 26DMK551, 26EBN087, 26FMC227

Product

Medline convenience kits labeled as: 1) LAVH, Medline Kit SKU CDS982273U; 2) GYN ABDOMINAL CDS, Medline Kit SKU CDS982654L; 3) GYN LAP HYSTERECTOMY CDS, Medline Kit SKU CDS982662Q; 4) CMH VAG HYSTERECTOMY PK-LF, Medline Kit SKU DYNJ54382F; 5) A P RESECTION, Medline Kit SKU DYNJ903467L.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3027-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.