Medline Convenience kits labeled as: 1) KIT GENERAL CLOSURE — Class II medical device recall Z-3028-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-09-18. Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. L
| Recall number | Z-3028-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-04-08 |
| Classified | 2024-09-06 |
| Reported by FDA | 2024-09-18 |
| Reason classes | packaging, device malfunction |
| Lot numbers | 21JBJ528, 21JBR416, 21JBR532, 21LBD248, 21LBH077, 22ABU681, 22ABW610, 22BBH582, 22BBP538, 22DBL196, 22EBP025, 22FBT088, 22FBT303, 22FBV156, 22GBD888, 22GBL911, 22GBU753, 22GBV087, 22GME957, 22HBA077, 22HBG952, 22HBJ926, 22HBN609, 22JBN831, 22JBP791, 22JME303, 22JMG284, 22KBD675, 22KBG540, 22KBU033, 22LBH669, 22LBJ084, 22LBJ768, 22LBM554, 22LBO669, 22LBS274, 22LMA157, 23ABG899, 23ABL575, 23ABS718 and 126 more |
Product
Medline Convenience kits labeled as: 1) KIT GENERAL CLOSURE , Pack Number DYKMBNDL200A ; 2) KIT GENERAL CLOSURE , Pack Number DYKMBNDL200AH; 3) CUST CHEST TUBE INSERTION X , Pack Number DYNDA2415B ; 4) LACERATION TRAY , Pack Number DYNDL1495A ; 5) LACERATION TRAY , Pack Number DYNDL1495AH; 6) LACERATION TRAY , Pack Number DYNDL1807B ; 7) LACERATION WITH INSTMTS TRAY, Pack Number DYNDL1963; 8) LACERATION WITH INSTMTS TRAY, Pack Number DYNDL1963H ; 9) LACERATION TRAY , Pack Number DYNDL1965A ; 10) STERILE RESUTURE PACK, Pack Number DYNDL1980A; 11) STERILE RESUTURE PACK, Pack Number DYNDL1980AH; 12) LACERATION TRAY , Pack Number DYNDL1981; 13) LACERATION TRAY , Pack Number DYNDL1985; 14) SUTURE TRAY , Pack Number DYNDL1986; 15) FGH FLOOR KIT , Pack Number DYNDL1989; 16) LACERATION KIT, Pack Number DYNDL1991; 17) LACERATION KIT, Pack Number DYNDL1992; 18) LACERATION KIT, Pack Number DYNDL1992H ; 19) ER LACERATION TRAY, Pack Number DYNDL1993; 20) LACERATION TRAY , Pack Number DYNDL1994; 21) CLOSURE PACK-LF , Pack Number DYNJ0807503N ; 22) CLOSING BUNDLE, Pack Number DYNJ52157I ; 23) PREMIUM CLOSUREPLUS PACK, Pack Number DYNJ54326A ; 24) ABD CLOSURE PACK, Pack Number DYNJ56987C ; 25) CLOSING PACK, Pack Number DYNJ57577A ; 26) SURGERY CLOSING KIT , Pack Number DYNJ67429B ; 27) CLOSING PACK, Pack Number DYNJ68267B ; 28) MICRODISECTOMY PACK , Pack Number DYNJ80585B ; 29) PREP TRAY , Pack Number DYNJRA1583D; 30) NECESSAIRES A POINT DE SUTURES, Pack Number M101498; 31) MAJOR LACERATION PACK-LF, Pack Number PHS751688G; 32) IR SUTURE PACK-LF , Pack Number PHS863717D ; 33) FINE LACERATION KIT , Pack Number SUT17215A; 34) MINOR LACERATION TRAY , Pack Number SUT18200 ; 35) LACERATION TRAY, Pack Number SUT20285A; 36) LACERATION TRAY W/ LIDOCAINE, Pack Number SUT20595A; 37) SNAG FREE LACERATION TRAY, Pack Number SUT21665; 38) LACERATION TRAY , Pack Number SUT21710 ; 39) LACERATION REPAIR TRAY, Pack Number SUT21780 ; 40) SNAG FREE LACERATION TRAY , Pack Number SUT21825
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-3028-2024. 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.