Data Foundry

Medical device recalls 2022

Medline Convenience kits labeled as: a — Class II medical device recall Z-1474-2022

Ongoing recall by MEDLINE INDUSTRIES, LP - SPT, reported 2022-08-03, distributed nationwide. Kits contain leaking bottles of isopropyl alcohol

Recall numberZ-1474-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - SPT, Waukegan, IL, United States
Recall initiated2022-06-06
Classified2022-07-27
Reported by FDA2022-08-03
DistributedNationwide (US)
Quantity6,569 units
Reason classespackaging
Lot numbers19HBE998, 19HBK745, 21CBT064, 21CBZ524, 21CBZ538, 21CBZ815, 21CDC622, 21DBE917, 21DBJ932, 21DBV520, 21EBI098, 21EDA769, 21EDC220, 21FBG162, 21FBQ232, 21GBC672, 21GBI192, 21GBM221, 21GBQ268, 21GDB289, 21GDC682, 21HBB233, 21HBG594, 21HBI534, 21HBQ840, 21HDC822, 21IBT387, 21IDA570, 21JBA902, 21JDA064, 21KBS110, 21LBB378, 21LBO497, 21LBO625, 21LBX041, 21LDA151, 21VBB580, 21VBC259, 22ABK810, 22ABO583 and 15 more
Model numbersCDS981543D, DYKM1875, DYKMBNDL142A, DYKS1185A, DYNJ0842793F, DYNJ0843063J, DYNJ901205C, DYNJ904395F, DYNJ905855, DYNJ906653A, P922260, PHS110395003

Product

Medline Convenience kits labeled as: a. MAJOR VASCULAR CDS, b. POST OP KIT, c. KIT NEURO FUS LUM POST SANSUR, d. KIT NEURO FUS LUM POST SANSUR , e. PRE-OP ACCESSORY KIT CHOICE, f. DEEP BRAIN STIMULATION PACK, g. DEEP BRAIN STIMULATION PACK, h. MINIMALLY INVASIVE PACK-LF, i. EVLP Pack/Kit, j. GENERAL PURPOSE CV, k. GENERAL PURPOSE CV, l. KIT GERMANTOWN CABG, m. KIT GERMANTOWN CABG, n. DENTAL RESTORATIONS, o. ALCOHOL PREP PACK, p. ALCOHOL PREP PACK, q. MATRIXECTOMY PACK-LF Model/Catalog Number: a. CDS981543D, b. DYKM1875, c. DYKMBNDL142A, d. DYKMBNDL142A, e. DYKS1185A, f. DYNJ0842793F, g. DYNJ0842793F, h. DYNJ0843063J, i. DYNJ901205C, j. DYNJ904395F, k. DYNJ904395F, l. DYNJ905855, m. DYNJ905855, n. DYNJ906653A, o. P922260, p. P922260, q. PHS110395003

Reason for recall

Kits contain leaking bottles of isopropyl alcohol

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-1474-2022. 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.