Public recall detail

Medline Neuro Sponges

2026-04-09

medium
General and plastic surgery Sterility
Quick summary

Quick summary: Medline Neuro Sponges. Reason: Sterility. Category: General and plastic surgery. Date: 2026-04-09.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Medline Neuro Sponges. Reason: Sterility. Category: General and plastic surgery. Date: 2026-04-09.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandMedline Industries, Lp
ProductMedline Neuro Sponges
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-81871

Affected products

ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG05
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG02
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG13
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG06
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG07
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG14
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG09
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable
ProductGauze Sponges, X-Ray Detectable
LotAll lots.
ModelNEUROSPNG11
Serial numberAll lots.
DescriptionGauze Sponges, X-Ray Detectable

Issue

Specific item(s) and lot(s) of Medline neuro sponges are recalled due to a potential out-of-specification for endotoxin. Elevated endotoxin levels may present potential health risks that could require medical or surgical intervention. The likelihood of adverse health consequences is considered remote. Customers are advised to destroy the recalled products.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesMedline Industries, LP Three Lakes Drive, Northfield, Illinois, United States, 60093
Recall date2026-03-30
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81871
Background{}
CompaniesMedline Industries, LP Three Lakes Drive, Northfield, Illinois, United States, 60093
AudiencesGeneral public Healthcare Industry
Source updated2026-04-09

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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