Medline Convenience Kits containing BD ChloraPrep Clear — Class II medical device recall Z-3073-2026
Ongoing recall by Medline Industries, LP, reported 2026-09-09, distributed nationwide. Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the ma
| Recall number | Z-3073-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-07-20 |
| Classified | 2026-08-31 |
| Reported by FDA | 2026-09-09 |
| Distributed | Nationwide (US) |
| Quantity | 222,653 total |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10195327400958, 10195327407094, 10195327502492, 10195327502614, 10195327509873, 10195327662462, 10198459035715, 10198459106125, 10198459199608, 10198459199615, 10198459234965, 10198459244070, 10198459256967, 10198459658884, 10198459779251 |
| Lot numbers | 24HBV192, 24HBW237, 24IBE381, 24IBE469, 24IBI505, 24IBK131, 24IBK133, 24IBL908, 24IBV947, 24IMF148, 24JBA557, 24JBF575, 24JBI308, 24JBI310, 24JBK987, 24JBS022, 24KBB551, 24KBE072, 24KBH534, 24KBJ830, 24KBJ831, 24KBL250, 24KBN934, 24KBN937, 24LBD419, 24LBI545, 24LBI552, 24LBN283, 24LBP258, 24LBU139, 24LMG085, 24LMH506, 25ABC487, 25ABO282, 25AMH560, 25GBA905, 25GBI398, 25GBI401, 25GBQ023, 25GBT182 and 73 more |
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 for recall
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.
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-3073-2026. 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.