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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

5 recalls · page 1 of 1

Medical devices

Reported Nov 20, 2024

VYGON 100 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9601; An empty single-use pouch made of plastic intended to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Metrix Company

Matched: BrandA limited number of IV bags have been found to leak during filling.

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2019

SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 1500mL, (legless) REF 66615 - Product Usage: For use in an…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Metrix Company

Matched: BrandPotential for leaking product

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2019

The Metrix Company recalls Metrix, Baxter Empty IV flexible containers (bag) due to Potential for leaking of the IV bag at the chamber divider rod

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

The Metrix Company

Matched: Brand · Product · Product detailsPotential for leaking of the IV bag at the chamber divider rod

FDA (recalls & safety alerts)

Medical devices

Reported Oct 11, 2017

SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Metrix Company

Matched: BrandThe hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as…

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

AUTOCOMP6 XPS High Speed Compounder REF 58810

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Metrix Company

Matched: BrandAn issue was identified after a redesign of the auto compounding device. The compounder cannot meet the designed accuracy specification when…

7 more products in this recall

FDA (openFDA device enforcement)

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