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. 2,926 recalls have been distributed to California in the last 12 months.
Showing 17301–17320 of 30,923 recalls
Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...
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 Line Kit with Sharps Safety Features and Maximal Barrier...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 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: Spring-Wire Guide Introducer Catheter Assembly Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features 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: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NvisionVLE¿ Low-Profile Optical Probe Recalled by Ninepoint Medical Inc. Due...
The Issue: Distal tips of the probes may detach from the probe shaft during use.
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: 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: 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: 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: OviTex 1S Reinforced BioScaffold 4x8cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 18x22cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.