Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,413 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,413 in last 12 months

Showing 3906139080 of 49,677 recalls

Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Zimmer, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

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.

Class II — Potential Health HazardOngoing
DrugMarch 9, 2015· Navinta LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Pharmatech Llc

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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Pharmatech Llc

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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Southwestern 4oz Veggie Burger 36 count Net Wt 9 lb. 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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Chef's Line Black Bean Burger 36-4.25 oz Net Wt. 9 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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product...

The Issue: Fujifilm is conducting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a Recalled...

The Issue: Fujifilm is reporting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS ROC Crown Component 4UR (5/pk) Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Specialty MiniScope Mech. Set Size 18 Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Recalled by Specialty...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing