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. 1,047 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,047 in last 12 months

Showing 18301–18320 of 50,914 recalls

Medical DeviceJuly 8, 2020· New Wave Endo-Surgical, Corp.

Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...

The Issue: The plastic housing on the device may fracture

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2020· Mylan Institutional LLC

Recalled Item: Daptomycin for Injection Recalled by Mylan Institutional LLC Due to Presence...

The Issue: Presence of Particulate Matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 7, 2020· KIND LLC

Recalled Item: ***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted...

The Issue: Product contains undeclared sesame seeds.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2020· Lamb Weston Inc

Recalled Item: WinCo Foods Tater Bites Shaped Recalled by Lamb Weston Inc Due to Foreign...

The Issue: The Tater Bites product has the potential to be contaminated with foreign...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

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

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18CM) APPX 0.26ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way Recalled by ICU Medical,...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 13 IN (33cm) APPX 0.96 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 13 IN(33cm) APPX 1.0 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx 0.35 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 114" (290 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 26 IN(66cm) APPX 3.9 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: DISTALE - 203 cm (80") Bifuse Ext Set w/6 Gang 1o2 Manifold Recalled by ICU...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.26 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing