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. 2,420 recalls have been distributed to Oregon in the last 12 months.
Showing 41721–41740 of 50,914 recalls
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5% Dextrose and 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R Multiple Electrolytes Injection Type 1 Recalled by Hospira Inc....
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R pH 7.4 Multiple Electrolytes Injection Type 1 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hapi Pudding Recalled by J F C International Inc Due to Product's label...
The Issue: Product's label fails to declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trabecular Metal Tibial Impactor Replacement Pads. Product Usage: TM Tibial...
The Issue: To provide clarifying instructions relating to the assembly/disassembly of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads...
The Issue: To provide clarifying instructions relating to the assembly/disassembly of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE is updating the...
The Issue: GE is updating the Preventative Maintenance procedure and schedule, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima NM/CT 640 Recalled by GE Healthcare, LLC Due to GE is issuing this...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo NM615 Recalled by GE Healthcare, LLC Due to GE is issuing this recall...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia (including Infinia Recalled by GE Healthcare, LLC Due...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.