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. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 29301–29320 of 49,990 recalls
Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...
The Issue: Inadequate seal due to lack of adhesive glue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...
The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...
The Issue: Failed impurities/degradation specifications: This product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option 2 Recalled by L. Perrigo Company Due to Defective Container: Carton...
The Issue: Defective Container: Carton is missing the tablet blister strip and tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...
The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid...
The Issue: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...
The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 500 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE BURN SHEET Recalled by Dukal Corp. Due to Intact carton revealed...
The Issue: Intact carton revealed presence of shredded burn sheets
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.