Data Foundry

Medical device recalls 2023

DYND3000xxP Series — Class II medical device recall Z-2227-2023

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-08-02, distributed nationwide. The case and each (i.e. packet) labels for the DYND3000xxP series do not include an expiration date, however,

Recall numberZ-2227-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2023-03-28
Classified2023-07-21
Reported by FDA2023-08-02
DistributedNationwide (US)
Countries outside the USBM
Quantity9,945 units
Reason classeslabeling
UPC / GTIN / UDI-DI10193489010671, 10193489010688, 10193489010695, 10193489010701, 10193489010718, 10193489010725, 10193489010732, 20193489010678, 20193489010685, 20193489010692, 20193489010708, 20193489010715, 20193489010722, 20193489010739

Product

DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs

Reason for recall

The case and each (i.e. packet) labels for the DYND3000xxP series do not include an expiration date, however, the lubricating jelly (MDS032280) included in the DYNDP3000xxP series is labeled with an expiration date.

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-2227-2023. 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.