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. 2,486 recalls have been distributed to Oregon in the last 12 months.
Showing 24001–24020 of 50,914 recalls
Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Product Usage: The Proton Therapy System - Proteus Recalled by...
The Issue: There is a risk of detachment of the Compact Gantry Rolling Floor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned Recalled by...
The Issue: Record review found the several productions runs were processed using the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sea Salt Caramels Tumbled In Milk Chocolate Recalled by Moonstruck Chocolate...
The Issue: The Sea Salt Caramels Tumbled In Milk Chocolate is recalled due to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended...
The Issue: Potential for the software on Automated PD System cyclers which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...
The Issue: Potential for the software on Automated PD System cyclers which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...
The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monsel's (Ferric Subsulfate) Solution Recalled by Gordon Laboratories Due to...
The Issue: Superpotent Drug: contains higher levels of Iron than labeled.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...
The Issue: ProSun International LLC discovered discrepancies in their Quality Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...
The Issue: ProSun International LLC discovered discrepancies in their Quality Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 7-8 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 5-6 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 1-2 Recalled by Smith & Nephew,...
The Issue: Higher than anticipated occurrence of bone fracture during the use of the XR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...
The Issue: Product mix up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.