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.

49,990 total recalls
2,660 in last 12 months

Showing 30213040 of 49,990 recalls

Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2025· Abbott Medical

Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...

The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2025· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear 1mL Applicators Recalled by CareFusion 213, LLC Due to...

The Issue: Non-Sterility: contamination of Aspergillus penicillioides, due to breach in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Smiths Medical ASD, Inc.

Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Airway adapter does not meet specification and may break off when attaching...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Smiths Medical ASD, Inc.

Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Airway adapter does not meet specification and may break off when attaching...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2025· Johnson, S C and Son, Inc

Recalled Item: Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium...

The Issue: Chemical Contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2025· ICU Medical, Inc.

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2025· ICU Medical, Inc.

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Mislabeling

The Issue: Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2025· Johnson, S C and Son, Inc

Recalled Item: Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5% Recalled...

The Issue: Chemical Contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund