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. 2,856 recalls have been distributed to California in the last 12 months.
Showing 22201–22220 of 30,923 recalls
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...
The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigger-Better-Bladder With 3/8" ID tubing Recalled by Circulatory Technology...
The Issue: The seal between the balloon and the housing may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Gauze Sponges Recalled by Covidien LLC Due to Compromised sterility...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAK Liquid Acrylic Resin sold under the following labels: 1) Recalled by...
The Issue: Possible presence of foreign material (rust).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition: Intended to produce cross-sectional images of...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERION Unit (Vision Planner) Product Usage: The VERION Image Recalled by...
The Issue: Alcon is conducting a voluntary medical device correction of all VERION...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is Recalled by GE...
The Issue: Ferrous material in the SIGNA Pioneer Table Control Box (TCB) could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...
The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...
The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT-5100 (Epic 5100) and RT 3100 : Product Usage: Recalled by Nidek Inc Due...
The Issue: There has been a reoccurrence of an issue on the RT 5100 and RT 3100 of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.