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. 1,113 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,113 in last 12 months

Showing 23541–23560 of 56,506 recalls

Medical DeviceJuly 10, 2019· B. Braun Medical, Inc.

Recalled Item: CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183 Recalled by B. Braun...

The Issue: The filter capacity is not achieved due to damage of the filter membrane.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 10, 2019· LNK International, Inc.

Recalled Item: Equate Night-time Sleep Aide (Diphenhydramine HCl) Recalled by LNK...

The Issue: Microbial contamination of non-sterile product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...

The Issue: Failed dissolution specifications : failed results at the 3-month stability...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Peanut Butter Chocolate Chip Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· FoodScience Corporation

Recalled Item: DaVinci Laboratories of Vermont Omega 3-1 Recalled by FoodScience...

The Issue: Dietary supplement mislabeled, undeclared allergen.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Original Trail Mix Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Chocolate Coconut Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR The Simply Real Bar: Chocolate Coconut Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Superfood Slam Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Dolfin S.A.

Recalled Item: Dolfin Dark Chocolate with Pink Peppercorns Net Wt 2.47 oz (70g) Recalled by...

The Issue: Product may contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...

The Issue: Potential of an open port in the quench venting system when using the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...

The Issue: Potential of an open port in the quench venting system when using the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...

The Issue: Potential of an open port in the quench venting system when using the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...

The Issue: Potential of an open port in the quench venting system when using the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...

The Issue: The action has been initiated to address reports of burst balloons which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing