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. 3,047 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,047 in last 12 months

Showing 53215340 of 56,506 recalls

Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV 18X103MM- Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 18/23-25MMX12CM-- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 23/28MMX10CM- Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX PC ESOPH STENT 18/23MM X 153MM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV 18X153MM-Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO OTW PC 23MM X 15.0CM IN 18.5 F-Agile Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2024· CooperSurgical, Inc.

Recalled Item: Silver-Plated Copper Sims Uterine Sound Recalled by CooperSurgical, Inc. Due...

The Issue: During the manufacturing process the devices were laser-marked with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2024· Medtronic MiniMed, Inc.

Recalled Item: MiniMed 620G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2024· Beckman Coulter Inc.

Recalled Item: IMMAGE Immunochemistry Systems IGM Immunoglobulin M Reagent IGM Recalled by...

The Issue: Firm identified two lots of reagents that are not meeting the sensitivity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2024· Medtronic MiniMed, Inc.

Recalled Item: MiniMed Insulin Pump Device. MiniMed 670G Recalled by Medtronic MiniMed,...

The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2024· Inspire Medical Systems Inc.

Recalled Item: Inspire Model 4340 Respiratory Sensing Lead Recalled by Inspire Medical...

The Issue: Labeling error with a mismatch between the shelf box serial number label and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2024· Medtronic MiniMed, Inc.

Recalled Item: MiniMed 630G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2024· Inspire Medical Systems Inc.

Recalled Item: Inspire Model 4063 Stimulation Lead Recalled by Inspire Medical Systems Inc....

The Issue: Labeling error with a mismatch between the shelf box serial number label and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2024· CooperSurgical, Inc.

Recalled Item: Stainless Steel Sims Uterine Sound Recalled by CooperSurgical, Inc. Due to...

The Issue: During the manufacturing process the devices were laser-marked with the...

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

Class II — Potential Health HazardOngoing
DrugJuly 31, 2024· Granules Pharmaceuticals Inc.

Recalled Item: Gabapentin Tablets Recalled by Granules Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 31, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin Extended-Release Capsules Recalled by Glenmark Pharmaceuticals...

The Issue: Failed Dissolution Specifications: below specification results

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 30, 2024· Colonna Brothers Inc.

Recalled Item: Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25...

The Issue: Elevated lead levels in cinnamon

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 30, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...

The Issue: During manufacturing, the last three tests from the 160 test flex of lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing