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 22901–22920 of 56,506 recalls
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...
The Issue: Discrepancy between the correct expiration dates on the individual pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Recalled by Enztec Limited Due to The femoral impactors have a higher than...
The Issue: The femoral impactors have a higher than normal risk of the arm breaking....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frozen Whole Yellow Tail Fusiler-200 Up Recalled by Foremost Foods...
The Issue: FDA product due to Salmonella were mistakenly distributed to a retail...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...
The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9646 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.