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. 1,804 recalls have been distributed to Oregon in the last 12 months.
Showing 39801–39820 of 50,914 recalls
Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...
The Issue: A wire component on the distal grasping assembly of the device became detached..
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Persona¿ Anterior Sizer with Locking Boom The Recalled by...
The Issue: Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Sizer with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Poly Vitamin Liquid with Iron Recalled by Pharmatech Llc Due to...
The Issue: Packaging label does not match individual product labeling. Outside...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rugby Poly Vitamin Liquid Recalled by Pharmatech Llc Due to Packaging label...
The Issue: Packaging label does not match individual product labeling. Outside...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Guiltless Gourmet Southwestern Veggie Burger 2.5oz 48 pieces Distributed by:...
The Issue: Products may contain cumin which may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Black Bean Burger 4.5 oz 40 pieces Net Wt. 11.25 Recalled by Cuisine...
The Issue: Products may contain cumin which may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.