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. 1,069 recalls have been distributed to Iowa in the last 12 months.
Showing 14541–14560 of 49,990 recalls
Recalled Item: Target Good & Gather Coconut Pineapple Sparkling Water 8 pack Recalled by...
The Issue: The company has received off flavor and off aroma complaints identified with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 Recalled by KEURIG DR PEPPER...
The Issue: The company has received off flavor and off aroma complaints identified with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg Recalled by...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: North by Honeywell PAIN STOPPER EXTRA STRENGTH (Acetaminophen 250 mg...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skinny Needle with Chiba Tip. RPN 090010 Recalled by Cook Inc. Due to...
The Issue: Specific lots may contain black debris on the exterior of the inner stylet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL ReadiPlasTin (20 mL) Recalled by Instrumentation Laboratory Due to...
The Issue: The firm has received customer reports of performance issues with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno with software VE20C- diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager application software (D00U005)...
The Issue: The processing of collected episode data may fail due to a software error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor with software VE20C-diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane with software VE20C-diagnostic imaging angiography...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion kits Recalled by Medtronic Perfusion Systems Due...
The Issue: Product is labeled as non-pyrogenic but endotoxin testing was not performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine...
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.