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. 3,026 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,026 in last 12 months

Showing 82218240 of 30,923 recalls

Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 1ml Code: OT01 Recalled by Medicina Uk Ltd Due to...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 2.5ml Code: OTH25 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 Recalled by Medicina...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 2.5ml Code: OT25 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 1ml Code: OTH01 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD Recalled...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2022· Intuitive Surgical, Inc.

Recalled Item: Da Vinci S/Si Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Due to the potential for unexpected motion caused by the partial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2022· Intuitive Surgical, Inc.

Recalled Item: Da Vinci X/Xi Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Due to the potential for unexpected motion caused by the partial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2022· Micro Therapeutics, Inc.

Recalled Item: Echelon -14 Recalled by Micro Therapeutics, Inc. Due to Outer carton...

The Issue: Outer carton packaging of microcatheters were exposed to wet substance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2022· Micro Therapeutics, Inc.

Recalled Item: Echelon -14 Micro Catheter Recalled by Micro Therapeutics, Inc. Due to Outer...

The Issue: Outer carton packaging of microcatheters were exposed to wet substance...

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· 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· 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· 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· 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· 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· 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
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