FDA Device recall Z-3070-2026
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 D…
- FDA Device
- Class II
- ongoing
- Published 2026-09-09
On 2026-09-09 the FDA classified a Class II recall of Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 D… by Medline Industries, citing convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the ap….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3070-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-20 |
| Published | 2026-09-09 |
| Last updated | 2026-09-23 05:30 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 DRAWER #4 ACC010479A DRAWER 2 ACC010690 ACC010875 DRAWER 3 SYR/DRS/MON/NG 1 OF 3 ACC011073 DRAWER 4 CIRCULATION ACC011088 DRAWER 5 - LEFT BOX ACC011067 LABOR TRIAGE KIT - LF #13232 DYKM1564 DYKM1564A LINEN UNIVERSAL PACK DYNJT10325 MAC KIT DYKS1089B NICU LINE PACK DYNJ63410 PEDIATRIC BLOOD CULTURE KIT DYNDH1363 RRMC CODE CART DRAWER 3 ACC010770 STANFORD TIME TO POSITIVITY DYNDH1591 STUDENT PRACTICE BAG W LOGO EDUC1043 EDUC1043A SUTURED SHEATH W/SCI #113198 DYKM1496 IV START KIT DYNDV2520
Reason
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.
Identifiers
| code_info | DYNDV1875 UDI-DI 10888277860209 Lot 24JMB689 ACC010972 UDI-DI 10198459303289 Lots 25DDA151 25DDA401…DYNDV1875 UDI-DI 10888277860209 Lot 24JMB689 ACC010972 UDI-DI 10198459303289 Lots 25DDA151 25DDA401 25EDA655 ACC010479A UDI-DI 10195327131517 Lot 25BDB620 ACC010690 UDI-DI 10195327433307 Lots 24LDB023 25BDA230 25GDA245 25JDB903 25KDB182 25LDA088 25LDA809 26ADC073 26CDA991 26DDB182 26EDA950 26EDB485 26FDB456 ACC010875 UDI-DI 10198459113659 Lots 24JDA648 25CDB776 25JDB205 25KDB028 25LDB271 26DDA182 26DDA786 26EDA629 ACC011073 UDI-DI 10198459569333 Lot 25LDA072 ACC011088 UDI-DI 10198459589577 Lots 26BDA548 26GDA090 ACC011067 UDI-DI 10198459529184 Lots 25KDA639 25LDA980 26CDB158 DYKM1564 UDI-DI 10889942754571 Lots 24HBW937 24JBX634 24LBR085 25GBH209 25IBK590 25LBD525 26ABI524 26BBM585 26DBC555 DYKM1564A UDI-DI 10198459805165 Lot 26FBK649 DYNJT10325 UDI-DI 10198459787324 Lots 26EBM250 26FBA470 26FBF055 26FBH553 26FBH554 DYKS1089 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-15 05:30 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3070-2026%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.