Data Foundry

Medical device recalls 2024

Medline procedural kits labeled as: 1) BOTOX KIT — Class II medical device recall Z-2750-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-09-04. Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. L

Recall numberZ-2750-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2024-04-08
Classified2024-08-28
Reported by FDA2024-09-04
Reason classespackaging, device malfunction
Lot numbers21ABM981, 21BBR866, 21FBI191, 21FBO406, 21FBR340, 21GDC910, 21JDA096, 22CDC307, 22DBH342, 22DBI420, 22DBI980, 22FBM439, 22KBD028, 22OBL867, 23BDC115, 23EDC523, 23GDA856, 23GMI735, 23HBM696, 23HBV422, 23IBC085, 23JBC148, 23JDA299, 23JDB728, 23KBK942, 23KMC310, 23LBA443, 24ABL480, 24ABM251, 24ABY049, CMPJ05506F, DYKM2000, DYNJ0608555P, DYNJ38988J, DYNJ47842C, DYNJ65156, DYNJ82179A, DYNJ82179AH, DYNJ901206F, DYNJ902703K

Product

Medline procedural kits labeled as: 1) BOTOX KIT - CHRONIC MIGRAINE, Pack Number DYKM2000; 2) BREAST, Pack Number DYNJ902703K; 3) ENT TYMPANOPLASTY PACK-LF , Pack Number DYNJ38988J; 4)FREE FLAP TRAM ADD ON PACK, Pack Number DYNJ82179A; 5) FREE FLAP TRAM ADD ON PACK, Pack Number DYNJ82179AH; 6) JSI-MUSCLE&PLASTICS PACK-LF , Pack Number DYNJ0608555P; 7) OCCULAR PLASTIC, Pack Number DYNJ901206F; 8) OCCULAR PLASTIC PACK, Pack Number CMPJ05506F; 9) OCCULOPLASTIC PACK, Pack Number DYNJ65156; 10) PLASTIC PACK, Pack Number DYNJ47842C;

Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

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-2750-2024. 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.