Data Foundry

Medical device recalls 2023

(1) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546C, 6… — Class II medical device recall Z-1162-2023

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-03-01, distributed nationwide. The convenience trays had improper placement of some of the components that were in the nonsterile portion of

Recall numberZ-1162-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2022-12-27
Classified2023-02-23
Reported by FDA2023-03-01
DistributedNationwide (US)
Quantity720 trays
Reason classessterility
UPC / GTIN / UDI-DI40195327069286, 40889942055518
Lot numbers20JBT517, 20KBD323, 20WBB357, 20XBC895, 21BBS043, 21BBS824, 21CBY712, 21GBH194, 21HBM415, 21IBW034, 21JBU806, 21KBE911, 22CBJ633
Model numbersDYNJ0248546C, DYNJ0248546D
Expiration dates2021-12-31, 2022-08-31, 2022-09-30, 2022-12-31, 2023-03-31

Product

(1) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546C, 6 kits per case, contains BD Chloraprep Hi-Lite Orange, 10.5 mL Applicator, Vendor PN: 930715NS; (2) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546D, 6 kits per case, contains BD Chloraprep Hi-Lite Orange, 10.5 mL Applicator, Vendor PN: 930715NS.

Reason for recall

The convenience trays had improper placement of some of the components that were in the nonsterile portion of the tray, thus, not receiving sterilization.

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-1162-2023. 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.