FDA Device recall Z-3073-2026
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE 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 ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE 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-3073-2026 |
| 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 ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE DYNDH1866 BLOOD CULTURE KIT DYNDH1462B DYNDH1622C DYNDH1622D DYNDH1622F DYNDH1715B DYNDH2028 DYNDH2048 BLOOD CULTURE-NB DYNDH2089 BLOOD DRAW KIT DYLAB1081 FLOORS BLOOD DRAW KIT DYLAB1080 PEDS BLOOD CULTURE KIT DYNDH1445C PERIPHERAL BLOOD CULTURE KIT DYNDH2350 WICHITA BLOOD CULTURE COLLECT DYNDH2093
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 | DYNDH1444D UDI-DI 10195327502492 Lots 24IBK133 24KBE072 24LBD419 25GBT189 25IME347 25IMI389 25KMA880…DYNDH1444D UDI-DI 10195327502492 Lots 24IBK133 24KBE072 24LBD419 25GBT189 25IME347 25IMI389 25KMA880 25KME693 26BMH685 26CMH411 26DME199 26EMB070 26EMF542 26FMC275 DYNDH1866 UDI-DI 10195327400958 Lots 24HBW237 24IBI505 24JBI308 24KBH534 24LBI545 25ABC487 25ABO282 DYNDH1462B UDI-DI 10195327662462 Lots 24HBV192 24IBE469 24IBV947 24JBA557 24JBI310 24KBJ830 24KBJ831 24KBN934 24LBN283 24LBP258 DYNDH1622C UDI-DI 10195327509873 Lots 24IBE381 24IBL908 24JBF575 24JBS022 24KBN937 24LBI552 DYNDH1622D UDI-DI 10198459234965 Lots 25GBA905 25GBI398 25GBT182 25HBN203 25IBH345 25IBQ486 25IBS192 25JBN629 25KBK718 25LBI568 DYNDH1622F UDI-DI 10198459658884 Lots 26BBL477 26CBA407 26CBD376 26DBA855 26DBL286 26FBF458 DYNDH1715B UDI-DI 10195327407094 Lot 24IMF148 DYNDH2028 UDI-DI 10198459035715 Lot 24KBL250 DYNDH2048 UDI-DI 10198459106125 Lots 24JBK987 |
|---|
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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FDA Device · Class II · 2026-09-30 · Medline Industries - Medline Convenience Kits: 1) MAJOR NEURO VCH, Catalog Number: DYNJ39218I
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3073-2026%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.