medical MODERATE Updated 2026-05-06

Medline Industries, LP recalls Medline medical procedure kits, containing Medline Neuro Spo

See all recalls from Medline Industries, LP →

Recalled Product

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINAL FUSION, Medline Kit Number/SKU CDS860017AG

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

Issued by

FDA

Distribution: Worldwide distribution.
Lot/Code Info: UDI/DI each 10198459237317, UDI/DI case 40198459237318: Lot Numbers: 25LBI308, 25JBH227, 25HBQ371, 25HBP069, 25GBQ494, 25FBM672, 25CBF603, 25BBG224, 25ABN190, 25ABN214.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Medline medical procedure kits, →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Philips North America recalls Philips SmartPath to dStream for 1.5T with MR Elastography (

2026-05-06 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Pa

2026-05-06 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

Philips North America recalls Philips SmartPath to dStream for XR and 3.0T with MR Elastog

2026-05-06 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

Medline Industries, LP recalls Medline and Centurion medical procedure kits, containing Med

2026-05-06 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.