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. 1,100 recalls have been distributed to Iowa in the last 12 months.
Showing 8901–8920 of 49,990 recalls
Recalled Item: Travoprost Ophthalmic Solution Recalled by Golden State Medical Supply Inc....
The Issue: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: enterade Advanced Oncology Formula Recalled by ENTRINSIC HEALTH SOLUTION INC...
The Issue: Potential for the product to develop mold and spoil.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NeuMoDx Cartridge-used for extraction Recalled by NeuMoDx Molecular Inc Due...
The Issue: Top label on some of the NeuMoDx cartridges within these lots may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-PRO 2- A powered ambulance cot that consists of a platform Recalled by...
The Issue: Base leg assembly may bend and result in difficulty engaging/disengaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA GBM Wells Recalled by Phadia Ab Due to Complaints that specific samples...
The Issue: Complaints that specific samples produced false positive EliA GBM results. A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH)...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Distal Probe. Used in Fluorescence in situ hybridization (FISH) Recalled...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible out...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Meshed Recalled by TEI Biosciences, Inc. Due to Possible out...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Ag Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 4.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 3.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Ag Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile CirClamp with 1.45cm Bell Reprocessed Recalled by MEDLINE...
The Issue: The kits incorrectly contain CirClamp subassembly 345CRSAK which results in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 2.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend MP Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.