Data Foundry

Medical device recalls 2023

Medline Probe Cover Kits containing sterile Ultrasound Gel — Class II medical device recall Z-2172-2023

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-07-26, distributed nationwide. Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

Recall numberZ-2172-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2023-05-18
Classified2023-07-20
Reported by FDA2023-07-26
DistributedNationwide (US)
Countries outside the USAE, CA, CN, CR, IN, LB, PA, QA, SA, SG
Quantity1,861 units
UPC / GTIN / UDI-DI10080196787692, 10193489278064, 10193489454536, 10195327071868, 10195327143046, 10195327176785, 10195327307011, 10195327319991, 40080196787693, 40193489278065, 40193489454537, 40195327071869, 40195327143047, 40195327176786, 40195327307012, 40195327319992
Model numbersCDS983069I, DYNJ30245, DYNJ47716B, DYNJ63347A, DYNJ63634A, DYNJ81389A, DYNJ83960, DYNJ907206D

Product

Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CHP COCHLEAR SUPPLEMENT CDS, Model Number CDS983069I; b) HEAD AND NECK PACK, Model Number DYNJ30245; c) IR THYROID PACK (THLUF)642-LF, Model Number DYNJ47716B; d) CENTRAL LINE INSERTION, Model Number DYNJ63347A; e) TAVR FAIRFAX, Model Number DYNJ63634A; f) PARATHYROID PACK, Model Number DYNJ81389A; g) THYRIOD PACK, Model Number DYNJ83960; h) WMC COCHLEAR IMPLANT ADD ON, Model Number DYNJ907206D

Reason for recall

Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

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-2172-2023. 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.