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. 2,989 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,989 in last 12 months

Showing 1286112880 of 56,506 recalls

DrugJune 29, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Testosterone Gel 1% (25mg testosterone/2.5g of gel) 2.5 g per unit dose...

The Issue: Superpotent Drug: Out of specification assay result was obtained during...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Eco Lips, Inc

Recalled Item: Juice Beauty Recalled by Eco Lips, Inc Due to Failed Dissolution Specifications

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 29, 2022· Eco Lips, Inc

Recalled Item: Juice Beauty Recalled by Eco Lips, Inc Due to Failed Dissolution Specifications

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 29, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Aspirin and Extended-Release Dipyridamole Capsules Recalled by Glenmark...

The Issue: Failed Tablet/Capsule Specification : Capsule breakage

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 29, 2022· OrthoPediatrics Corp

Recalled Item: Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN...

The Issue: Manufacturing variance near transition of tip is increasing the likelihood...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Biosense Webster, Inc.

Recalled Item: CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath Recalled by Biosense...

The Issue: Outside packaging for a device indicated for introducing cardiovascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Trinity Sterile, Inc.

Recalled Item: Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708...

The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Trinity Sterile, Inc.

Recalled Item: Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Recalled by...

The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Trinity Sterile, Inc.

Recalled Item: Wolf Pak Premium Dressing Change Kit with Statlock CS/30 Recalled by Trinity...

The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Trinity Sterile, Inc.

Recalled Item: Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Recalled by Trinity...

The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES Recalled by MEDLINE INDUSTRIES,...

The Issue: stability failure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE Measured Sizing and Rotation Guide-to size the femur and Recalled by...

The Issue: Manufactured with a Galvanized High Carbon Steel spring instead of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· SONEX HEALTH LLC

Recalled Item: SX-One MicroKnife Recalled by SONEX HEALTH LLC Due to Potential of dull blade

The Issue: Potential of dull blade

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2022· Vi-Jon, LLC

Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...

The Issue: Cross Contamination With Other Products: Product is cross contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 28, 2022· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist Device (HVAD) System Batteries Recalled by...

The Issue: Battery performance issues. Battery electrical faults render it unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use Recalled by...

The Issue: Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Valor Compounding Pharmacy, Inc DBA Valor Compounding Pharmacy

Recalled Item: Nifedipine WSP 0.2% Ointment Recalled by Valor Compounding Pharmacy, Inc DBA...

The Issue: Subpotent and Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund