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. 2,669 recalls have been distributed to California in the last 12 months.
Showing 41301–41320 of 56,506 recalls
Recalled Item: Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...
The Issue: Unexpected rate of postoperative fractures resulting in the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiographic Injector. Medrad Mark 7 Arterion Injection System Recalled by...
The Issue: Software Version SW 005.006_SH, resulted in the removal of purge enforcement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...
The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rivastigmine Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically Recalled...
The Issue: The pH level in coffee product was elevated above 4.6.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baby Bruddah's Chocolate Mac Nut Buttah. 12 oz. container Recalled by Mahina...
The Issue: IEH sample of macadamia nuts was found positive for Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Izzie Macs! Macadamia Nuts Recalled by Mahina Mele Farm Due to Potential...
The Issue: IEH sample of macadamia nuts was found positive for Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Izzie Macs! Macadamia Nuts Recalled by Mahina Mele Farm Due to Potential...
The Issue: IEH sample of macadamia nuts was found positive for Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Izzie Macs! Macadamia Nuts Recalled by Mahina Mele Farm Due to Potential...
The Issue: IEH sample of macadamia nuts was found positive for Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baby Bruddah's Mac Nut Buttah. 12 oz. container Recalled by Mahina Mele Farm...
The Issue: IEH sample of macadamia nuts was found positive for Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ferno iNX Wheeled Stretcher Recalled by Ferno-Washington Inc Due to Hole...
The Issue: Hole elongation in the telescoping load frame channel. A hole elongation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemocor High Performance Hemoconcentrator Recalled by Medivators, Inc. Due...
The Issue: Hemoconcentrators may exhibit low ultrafiltration performance that is below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer....
The Issue: Flow restriction issues in a trifurcated IV set included in the pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...
The Issue: Potential to improperly characterize tissue within the jaws, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 Recalled by Trilliant Surgical Ltd. Due to Gridlock screw driver bits...
The Issue: Gridlock screw driver bits for the Gridlock Plating System were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.