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. 2,819 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,819 in last 12 months

Showing 3388133900 of 56,506 recalls

Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2017· Philips Visicu

Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...

The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2017· Myelotec, Inc.

Recalled Item: Myelotec Video Guided Catheters Recalled by Myelotec, Inc. Due to...

The Issue: Obstructed/blocked port from defective VGC Access Port Body component.

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2017· Fougera Pharmaceuticals Inc.

Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...

The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 2, 2017· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: Ortho Kinematics notified customers that errors were contained in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2017· Roche Diagnostics Corporation

Recalled Item: Cobas 8100 uni-directional (BRF) module with Software Version 02-xx Recalled...

The Issue: Roche Diagnostics Corp. initiated a voluntary correction because a rack...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2017· Roche Diagnostics Corporation

Recalled Item: Cobas 8100 bi-directional (BRF) module with Software Version 02-xx Recalled...

The Issue: "Roche Diagnostics Corp. initiated a voluntary correction because a rack...

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

Class II — Potential Health HazardOngoing
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: BRAISED BAMBOO SHOOT TIPS 10 oz. cans Recalled by Companion Foods Corp. Due...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: BRAISED BEAN CURD (MOCK CHICKEN)10 oz. cans Recalled by Companion Foods...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: SZECHUAN STYLE KUNG-PAO SAUCE (HOT PAPAO LAJAN) Recalled by Companion Foods...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: VEGETARIAN TUNA FISH Recalled by Companion Foods Corp. Due to An FDA...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: BRAISED BAMBOO SHOOT TIPS WITH CHILI Recalled by Companion Foods Corp. Due...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: VEGETARIAN MINCED MEAT WITH SHIITAKE 5 1/3 oz.. cans Recalled by Companion...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2017· Bitterman and Sons

Recalled Item: Parmesan Truffle Salt. The product is packaged in glass taster Recalled by...

The Issue: Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2017· Companion Foods Corp.

Recalled Item: FAT-CHOY STYLE VEGETABLE SOUP Recalled by Companion Foods Corp. Due to An...

The Issue: An FDA inspection at the manufacturing facility found seven products that do...

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

Class III — Low RiskOngoing
Refund
DrugMarch 1, 2017· Signature Club A Ltd

Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...

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

Class II — Potential Health HazardOngoing
Refund