Data Foundry

Medical device recalls 2024

Centurion manual surgical kits labeled as: a) ST — Class II medical device recall Z-1442-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-04-10, distributed nationwide. Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The

Recall numberZ-1442-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2024-02-23
Classified2024-03-29
Reported by FDA2024-04-10
DistributedNationwide (US)
Countries outside the USCA, PA
Quantity7,950 units
Reason classessterility, packaging
UPC / GTIN / UDI-DI00653160028966, 00653160286540, 00653160290752, 00653160306552, 00653160337341, 00653160342291, 10193489191585, 10653160028963, 10653160286547, 10653160290759, 10653160306559, 10653160337348, 10653160342298, 20193489191582
Lot numbers2023022290, 2023041090, 2023041190, 2023042490, 2023052390, 2023062290, 2023070390, 2023081490, 2023101190, 2023101890, 2023103190, 2023112190

Product

Centurion manual surgical kits labeled as: a) ST. VIRTUS SPLINTER FORCEP 6" (SF8246), Product Code 66580; b) DEBRIDEMENT TRAY, Product Code I86630; c) BIOPSY INSTRUMENT PACK, Product Code I86690; d) DEBRIDEMENT TRAY, Product Code I86815; e) IR ADSON FORCEP & NEEDLE HOLDER, Product Code MNS12675; f) TOENAIL REMOVAL KIT, Product Code SUT20350 MEDLINE GENERAL PURPOSE INST. TRAY, Product Code DYNDA2346A

Reason for recall

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

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-1442-2024. 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.