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. 2,660 recalls have been distributed to Iowa in the last 12 months.
Showing 1561–1580 of 49,990 recalls
Recalled Item: MAC VU360 Acquisition Trunk Cable and Module Holder Recalled by GE Medical...
The Issue: If a user incorrectly places the Acquisition Module into the Acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyDay Toric Recalled by CooperVision, Inc. Due to One lot manufactured with...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant 1-Day Premium Toric Recalled by CooperVision, Inc. Due to One lot...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofmed Breathables Recalled by CooperVision, Inc. Due to One lot...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits: 1) VALVE PACK-LF Recalled by Medline Industries, LP Due to The...
The Issue: The kits contain certain lots of cannula products where the catheter may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venclose digiRF Generators Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Software version 3.35 of the Venclose digiRF Generator incorporates a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG6+ cartridge. List Number: 03P77-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz Recalled by...
The Issue: Mold. The firm noticed an increase in customer complaints. They conducted a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Northwind...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) Recalled by Baxter...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP Recalled by The Harvard Drug Group LLC dba Major...
The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.