Data Foundry

Medical device recalls 2026

Medline medical convenience kits — Class II medical device recall Z-2995-2026

Ongoing recall by Medline Industries, LP, reported 2026-09-02, distributed nationwide. Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurospon

Recall numberZ-2995-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-07-08
Classified2026-08-21
Reported by FDA2026-09-02
DistributedNationwide (US)
Quantity246 kits
Reason classessterility
UPC / GTIN / UDI-DI10195327123819, 10198459258961, 10198459372667, 10198459558757, 40195327123810, 40198459258962, 40198459372668, 40198459558758
Lot numbers23EBA762, 23HBG168, 23KBW672, 24ABD437, 24ABO388, 25FMD894, 25JMG396, 25JMH786, 25KMF523, 25KMF530, 26AMH848, 26CMD479

Product

Medline medical convenience kits, labeled as: 1) CRANIOTOMY PACK, Medline Kit SKU DYNJT6545; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ88056A; 3) ENT SINUS PACK, Medline Kit SKU DYNJ89001; 4) THYROID ENT, Medline Kit SKU DYNJ908641.

Reason for recall

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

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-2995-2026. 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.