Product Recalls in California
Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,774 recalls have been distributed to California in the last 12 months.
Showing 10321–10340 of 30,923 recalls
Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scooter Recalled by Merits Holdings Co. dba Merits Health Products, Inc. Due...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg MR Cannula Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Left Heart Kit 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: 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: 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: SoftGenomics version 4.1.15.6 SoftGenomics is a laboratory workflow and...
The Issue: Software showing wrong results reported, PDF not match HIS.
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: 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: 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: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...
The Issue: Software is given wrong results going out to HIS on test that had reruns.
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: Palm Cups - Product Usage: intended to be used to Recalled by Smiths Medical...
The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...
The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...
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: 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: 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: 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: 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: 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.