FDA Device recall Z-3059-2024
Medline Convenience kits, labeled as: 1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115
- FDA Device
- Class II
- ongoing
- Published 2024-09-18
On 2024-09-18 the FDA classified a Class II recall of Medline Convenience kits, labeled as: 1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115 by Medline Industries Northfield, citing 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 m….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3059-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-08 |
| Published | 2024-09-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | n/a |
Product
Medline Convenience kits, labeled as: 1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115; 2) NICU CNTRL LINE BLOOD DRAW KIT, Pack Number DYLAB1044; 3) NEURO ANGIO PACK, Pack Number DYNDA1431A; 4) BLOOD WITHDRAWAL KIT #2, Pack Number DYNDA1683A; 5) LCPH LAB DRAW KIT , Pack Number DYNDH1641A ; 6) LCPH LAB DRAW KIT , Pack Number DYNDH1641AH; 7) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798; 8) BLOOD CULTURE, Pack Number DYNDH1921; 9) BLOOD WITHDRAWAL TRAY, Pack Number DYNDV1588F; 10) BLOOD WITHDRAWAL TRAY , Pack Number DYNDV1588G ; 11) PHLEBECTOMY PK, Pack Number DYNJ84749; 12) ARTHROGRAPH TRAY, Pack Number MNS12670A; 13) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915; 14) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915H ; 15) LACERATION TRAY, Pack Number SUT20955
Reason
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.
Identifiers
| code_info | BP115, Lot Number 21BBG338 ; BP115, Lot Number 21CBE353 ; BP115, Lot Number 21CBJ050 ; DYLAB1044, Lot Number 23GBM78…BP115, Lot Number 21BBG338 ; BP115, Lot Number 21CBE353 ; BP115, Lot Number 21CBJ050 ; DYLAB1044, Lot Number 23GBM782 ; DYNDA1431A, Lot Number 2020012890; DYNDA1683A, Lot Number 2019011790; DYNDA1683A, Lot Number 2019032590; DYNDA1683A, Lot Number 2019042390; DYNDA1683A, Lot Number 2019072390; DYNDA1683A, Lot Number 2019090990; DYNDA1683A, Lot Number 2019102390; DYNDA1683A, Lot Number 2019112290; DYNDA1683A, Lot Number 2020030990; DYNDH1641A , Lot Number 21JBE248 ; DYNDH1641A , Lot Number 21JBY828 ; DYNDH1641AH, Lot Number 21JBE248 ; DYNDH1641AH, Lot Number 21JBY828 ; DYNDH1798, Lot Number 2022112990; DYNDH1921, Lot Number 23KBC196; DYNDV1588F, Lot Number 2019022090; DYNDV1588F, Lot Number 2019041890; DYNDV1588F, Lot Number 2019090390; DYNDV1588F, Lot Number 2020012890; DYNDV1588G , Lot Number 22GBL908 ; DYNDV1588G , Lot Number 22HBN586 ; DYNDV1588G , Lot Number 22JBI927 ; DYNDV1588G , Lot Number 22LBK218 ; DYNDV1588G , Lot Number 23ABJ940 ; DYNDV1588G , Lot |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3059-2024%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.