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. 2,662 recalls have been distributed to California in the last 12 months.
Showing 2641–2660 of 30,923 recalls
Recalled Item: X-Flow prostatectomy catheter Recalled by Coloplast Manufacturing US, LLC...
The Issue: A possible sterility issue was detected in Coloplast's facility on some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow P2Y12 Platelet Reactivity Test Recalled by Accriva Diagnostics,...
The Issue: Platelet Reactivity Test distributed without appropriate US-FDA market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemodynamics software Recalled by A L I...
The Issue: Software defect concerning autosave mechanism may result in the clinician...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo software Recalled by A L I Technologies Ltd Due to...
The Issue: Software defect concerning autosave mechanism may result in the clinician...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Folysil Silicone Foley Catheters Recalled by Coloplast Manufacturing US, LLC...
The Issue: A possible sterility issue was detected in Coloplast's facility on some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix...
The Issue: Incorrect expiration date listed on the outer box, which does not align with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoCove Putty Recalled by IsoTis OrthoBiologics, Inc. Due to Hydration...
The Issue: Hydration issue resulting in the product being less cohesive and moldable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Intact PTH assay Recalled by Beckman Coulter, Inc. Due to Beckman...
The Issue: Beckman Coulter has identified that some Access PTH reagent packs from lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number:...
The Issue: Elevated residues of anti-block/slip additive used in manufacturing found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...
The Issue: Due to an increase of complaints for bracket bond failures and skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Mini Enteral Extension Set Recalled by Applied Medical Technology Inc...
The Issue: The extension sets subject to this recall have ENFit connections, although...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code Recalled...
The Issue: Due to complaints received for the marker band detaching from the distal tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse PRO The Spacelabs model 98700 is a Recalled by Spacelabs Healthcare,...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.