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. 2,881 recalls have been distributed to California in the last 12 months.
Showing 19101–19120 of 30,923 recalls
Recalled Item: VASER Amplifier Recalled by Solta Medical Inc Due to Potential inaccurate...
The Issue: Potential inaccurate calibration by service depot repair, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...
The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE BURN SHEET Recalled by Dukal Corp. Due to Intact carton revealed...
The Issue: Intact carton revealed presence of shredded burn sheets
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftLab Software Laboratory information system to be used in a Recalled by...
The Issue: Display of lab results based on incorrect LOINC code/test descriptions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...
The Issue: Hub damage resulting in breakage and/or leakage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Logic Fit Tibial Tamp Head Recalled by Exactech, Inc. Due to The firm...
The Issue: The firm determined that the labeling (surgical technique) should be updated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...
The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38 Recalled by...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #:...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer Recalled by Exactech,...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.