Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,409 recalls have been distributed to Iowa in the last 12 months.
Showing 39141–39160 of 49,990 recalls
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: 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: 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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit Recalled by Specialty Appliance...
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.
Recalled Item: M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 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.