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. 2,551 recalls have been distributed to Iowa in the last 12 months.
Showing 16581–16600 of 49,990 recalls
Recalled Item: O Organics Plant Based Mushroom and Veggie Organic Burger Patties Recalled...
The Issue: Labeling error caused product to claim Gluten Free and Vegan when it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Wildtree***Leslies Chili Blend***Organic & Gluten Free***Net Wt. 3.7 oz....
The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Wildtree***Taco Seasoning***Organic & Gluten Free***Net Wt. 8...
The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...
The Issue: Product was compromised during shipment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...
The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...
The Issue: Superpotent Drug. Lidocaine higher concentration than listed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oseltamivir Phosphate for Oral Suspension Recalled by Lupin Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications; Out-of-specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RUFFLES "PARTY SIZE" ORIGINAL POTATO CHIPS 13 1/2 oz. Recalled by Frito-Lay,...
The Issue: Potential to contain undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. Recalled by...
The Issue: Retail Box did not contain list of ingredients or allergen statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...
The Issue: The text on the patient pack is correct and the product itself remains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...
The Issue: Product was distributed without receiving regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...
The Issue: Non-sterile product was shipped to customers labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.