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. 2,926 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,926 in last 12 months

Showing 1768117700 of 56,506 recalls

DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: ViCTOZA (liraglutide) injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Macleods Pharma Usa Inc

Recalled Item: Candesartan Cilexetil Tablets Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp PenFill (insulin aspart injection) 100 units/mL (U-100) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Levemir FlexTouch (insulin detemir) injection Recalled by Novo Nordisk Inc...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp (insulin aspart injection) Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp FlexTouch (insulin aspart injection) 100 units/mL (U-100) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 100 units/mL (U-100) Recalled...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: NovoLog (Insulin aspart) Injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 200 units/mL (U-200) Recalled...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2021· Avanti Frozen Foods Private Limited

Recalled Item: 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- Recalled by...

The Issue: One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· GE Healthcare, LLC

Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Baxter Healthcare Corporation

Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...

The Issue: Potentially defective component in the AC power adapter which may fail over...

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

Class II — Potential Health HazardOngoing