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. 1,118 recalls have been distributed to California in the last 12 months.
Showing 17301–17320 of 30,923 recalls
Recalled Item: ARROWg+ard Blue¿ PSI Kit with Integral Hemostasis Valve/ Side Port Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echogenic Introducer Needle Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Two-Lumen CVC Kit Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheath Adapter with Cath-Gard¿ Catheter Contamination Shield for use with...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...
The Issue: There is a supplier quality issue with the terminal blocks which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING Recalled by Smith &...
The Issue: A single lot of GENESIS II FEMORAL FIVE DEGREE VALGUS BUSHING due to a laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio-Seal Evolution Vascular Closure Device Recalled by Terumo Medical Corp...
The Issue: Two lots of product were released for distribution prior to the completion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.