DeviceSignal · Recall classified

Medline Industries, LP

FDA classified a device recall on 2026-08-31 · Class II · Z-3069-2026

EventRecall classified
Effective2026-08-31
ClassificationClass II

On 2026-08-31 the FDA classified a device recall from Medline Industries, LP as Class II. Product: Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN…. Recall Z-3069-2026. The firm initiated it on 2026-07-20. This reports the classification FDA published on that date.

Reported facts

Recall number
Z-3069-2026
Classification
Class II
Classified on
2026-08-31
Initiated on
2026-07-20
Firm
Medline Industries, LP
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.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DYNJ42828B EYE BASIN TRAY-LF DYNJ42832B

Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.

Provenance

Source
fda_device_enforcement
Source record
Z-3069-2026
Snapshot hash
e8e634c086f9f5f52e82a7eef6331d8800209bbb8cbb79bd654d29f1222caae4
Source URL
https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
Observed
2026-09-23T12:43:31.676Z
Transform
fda_device_enforcement_to_recall v1
Event rule
fda_device_recall_classified v1
Event key
6213dd2bfb9e2b4ab55cb42a3f54ed21cd6afd02b30f2d7bafae01222ae094e4
Signal type
device_recall.classified

Source terms that apply

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Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)