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. 1,774 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,774 in last 12 months

Showing 96019620 of 30,923 recalls

Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with Recalled by B. Braun...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: 60 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT FEM CUT TIB PIN R- TruMatch Patient Specific Recalled by DePuy...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the pump set...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Vitrectomy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Basic Cataract tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ear Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Measured Volume Solution Set/ w/ Auto Shut-Off. Single-use...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: 15 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Newborn Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing