Data Foundry

Medical device recalls 2024

MEDLINE convenience kits labeled as: 1) VAGINAL — Class II medical device recall Z-0641-2025

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-12-11, distributed nationwide. Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil wh

Recall numberZ-0641-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2024-10-09
Classified2024-12-05
Reported by FDA2024-12-11
DistributedNationwide (US)
Quantity1,952 units
UPC / GTIN / UDI-DI10193489265699, 10195327043766, 10195327200404, 10195327228002, 10195327273668, 10195327313302, 40193489265690, 40195327043767, 40195327200405, 40195327228003, 40195327273669, 40195327313303
Lot numbers22DMI812, 22FMC589, 22GBA249, 22HBC733, 22HBH633, 22JBF053, 22KBS878, 22LBL495, 23ABF616, 23ABF770, 23AMG530, 23AMH550, 23BBF607, 23BBH334, 23BBS154, 23CBC829, 23CBD779, 23CBU078, 23CBU862, 23DMD460, 23EBG938, 23EBU222, 23FBI028, 23FMI241, 23GBH707, 23GBI132, 23HBG687, 23HMI199, 23IBE467, 23IBF280, 23IMG365, 23JBE732, 23JMF359, 23KBA604, 23KBU446
Model numbersCDS984955M, CDS984995M, DYNJ0826768P, DYNJ59081C, DYNJ65807C, DYNJ67757B

Product

MEDLINE convenience kits labeled as: 1) VAGINAL, REF CDS984955M; 2) DAY SURG LARGE VAG CDS, REF CDS984995M; 3) MAJOR VAGINAL PACK-LF, REF DYNJ0826768P; 4) VAGINAL PACK, REF DYNJ59081C; 5)VAGINOPLASTY PACK, REF DYNJ65807C; 6) ACH MAJOR VAGINAL PACK, REF DYNJ67757B

Reason for recall

Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.

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-0641-2025. 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.