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. 1,172 recalls have been distributed to California in the last 12 months.
Showing 16301–16320 of 56,506 recalls
Recalled Item: Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretch Leveller Model Number: 3156200 - The combination of this Recalled by...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexoStretch Model Number: 3156057 - The combination of this products...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LikoStretch 1900 Model Number: 3156051 - The combination of this Recalled by...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OctoStretch with Stretch Leveller - The combination of this products...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC Recalled...
The Issue: Stretch Leveller has the potential to lose the function of maintaining a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydro Pinapple Burn Max Health Thach Dua Recalled by Ebay Seller - John...
The Issue: Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...
The Issue: Non-Sterility: firm's third party lab confirmed microbial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET82HP OUTLOOK PUMP EXTENSION SET-single-use for use with the Outlook...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...
The Issue: Software: A coding error associated with the Fast3D Segmentation software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTLOOK PUMP IV SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.