Recall Z-3069-2026
- Recall number
- Z-3069-2026
- Event number
- 99561
- Firm
- Medline Industries, LP
- Firm FEI
- 1417592
- Product code
- KDD
- Status
- Open, Classified
- Initiated
- 2026-07-20
- Posted
- 2026-08-31
- Root cause
- Nonconforming Material/Component
- 510(k) numbers
- K834532, K811855, K821814, K924117, K870373, K834135, K803199, K902441, K832628, K821501, K913049, K830374, K811086, K820423, K821502, K833075, K831841, K920516, K925215, K760051, K843115, K920763, K843206, K072814, K803119, K761193, K833438, K822158, K910369, K803118
Product#
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DYNJ42828B EYE BASIN TRAY-LF DYNJ42832B
Reason for Recall#
Downstream recall - manufacturer recalled specific lots of BD ChloraPrep Clear - 1mL Applicators. Affected product may exhibit an open or incomplete seal on the packaging of the applicator. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.