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. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 24812500 of 56,506 recalls

Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model Number 40KWFX Recalled by SEDECAL SA Due to Sedecal sent an email to...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model SM-32HF-Batt Recalled by SEDECAL SA Due to Sedecal sent an email to...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· SEDECAL SA

Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...

The Issue: Sedecal sent an email to its consignees to remind the users that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides Recalled by Ortho-Clinical Diagnostics,...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
FoodJune 6, 2025· August Egg Company

Recalled Item: --- Shell Eggs Recalled by August Egg Company Due to Potential Salmonella...

The Issue: Potential contamination with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 6, 2025· Church & Dwight Inc

Recalled Item: Orajel Baby Recalled by Church & Dwight Inc Due to Microbial Contamination...

The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 6, 2025· Church & Dwight Inc

Recalled Item: ZICAM COLD REMEDY MEDICATED NASAL SWABS Recalled by Church & Dwight Inc Due...

The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 6, 2025· Church & Dwight Inc

Recalled Item: ZICAM NASAL ALLCLEAR Recalled by Church & Dwight Inc Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 6, 2025· Boston Scientific Neuromodulation Corporation

Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...

The Issue: As a result of a comprehensive product performance review it was determine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2025· Bausch & Lomb Surgical, Inc.

Recalled Item: Akreos Recalled by Bausch & Lomb Surgical, Inc. Due to An off-power error...

The Issue: An off-power error was identified, which resulted in a diopter of 16, rather...

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

Class III — Low RiskOngoing