Medline medical convenience kits — Class II medical device recall Z-2996-2026

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 number	`Z-2996-2026`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	Medline Industries, LP, Northfield, IL, United States
Recall initiated	2026-07-08
Classified	2026-08-21
Reported by FDA	2026-09-02
Distributed	Nationwide (US)
Quantity	3,468 kits
Reason classes	sterility
UPC / GTIN / UDI-DI	`10193489232394`, `10193489863994`, `10193489880564`, `10193489887631`, `10195327090111`, `10195327123451`, `10195327281250`, `10195327452490`, `40193489232395`, `40193489863995`, `40193489880565`, `40193489887632`, `40195327090112`, `40195327123452`, `40195327281251`, `40195327452491`
Lot numbers	`22BME230`, `22CMA406`, `22DMH314`, `22EMB248`, `22EMB958`, `22EMC777`, `22EMI134`, `22FMB806`, `22HMB295`, `22HME564`, `22IMA455`, `22IMB860`, `22JMI068`, `22LMB601`, `22LME727`, `23AMH395`, `23AMJ022`, `23CMB364`, `23EMA407`, `23EMD743`, `23FMH669`, `23GMI744`, `23HBH164`, `23HBO192`, `23HBV863`, `23HMF326`, `23IBF802`, `23IBS028`, `23JBV613`, `23JME474`, `24ABN077`, `24ABN475`, `24BMI624`, `24DBA116`, `24DME519`, `24EME751`, `24EMG256`, `24GMJ491`, `24IMA243`, `24JMA162` and 9 more

Product

Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU DYNJ32770V; 3) NEURO BUNDLE-LF, Medline Kit SKU DYNJ40095D; 4) NEURO PACK-LF, Medline Kit SKU DYNJ42844D; 5) NEURO PACK, Medline Kit SKU DYNJ45121I; 6) NEURO LAMINECTOMY PACK, Medline Kit SKU DYNJ58012A; 7) NEURO PACK SJ, Medline Kit SKU DYNJ63477A; 8) BASIC NEURO PACK, Medline Kit SKU DYNJ83071A.

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-2996-2026. 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.