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. 2,457 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,457 in last 12 months

Showing 2946129480 of 50,914 recalls

DrugJune 12, 2017· Vi-Jon, Inc.

Recalled Item: Magnesium Citrate Saline Laxative Cherry Flavored Recalled by Vi-Jon, Inc....

The Issue: Presence of foreign substance: glass particle

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 12, 2017· Bolner's Fiesta Products, Inc

Recalled Item: Chili Pequino 0.25 oz packaged in a clear plastic bag Recalled by Bolner's...

The Issue: Low levels of peanuts detected

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Zimmer Biomet, Inc.

Recalled Item: DRILL BIT MINI QUICK CONNECT 1.0MM Recalled by Zimmer Biomet, Inc. Due to A...

The Issue: A raw material anomaly was discovered in four lots of raw material and has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Invuity, Inc.

Recalled Item: INVUITY(R) PhotonBlade(TM) Recalled by Invuity, Inc. Due to A small number...

The Issue: A small number of customer observations were recently received which related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...

The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...

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

Class II — Potential Health HazardOngoing
FoodJune 11, 2017· Fit and Focused Supplements

Recalled Item: FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj Recalled by Advanced...

The Issue: Subpotent Drug: found to be below the specification for labeled assay.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin 100 mcg/mL QS 5% Dextrose Inj Recalled by Advanced Pharma Inc....

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma Inc....

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...

The Issue: Subpotent Drug: found to be below the specification for labeled assay.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj Recalled by Advanced...

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

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

Class II — Potential Health HazardOngoing
Refund