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. 2,618 recalls have been distributed to Iowa in the last 12 months.
Showing 9801–9820 of 28,127 recalls
Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gang Cath Lab Set Recalled by Smiths Medical ASD Inc. Due to Specific lots...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK Recalled by Smiths...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE TUBING Recalled by Smiths Medical ASD Inc. Due to Specific...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 280 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD Recalled by Smiths Medical ASD Inc....
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...
The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...
The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...
The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.