Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,641 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,641 in last 12 months

Showing 76817700 of 28,488 recalls

Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2022· Carwild Corporation

Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...

The Issue: Sterility with new cotton source not validated

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites Recalled by...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· Randox Laboratories Ltd.

Recalled Item: The Randox Serology I Positive Control contains the following analytes...

The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 2 Needleless Y-Site Recalled by CAREFUSION...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 4-way stopcock Recalled by CAREFUSION Due to...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set Recalled by CAREFUSION Due to Administration set,...

The Issue: Administration set, and extension set product labels list expiration year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 8.5" (22 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx 0.84 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· MERCHSOURCE LLC

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing