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. 3,022 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,022 in last 12 months

Showing 94619480 of 56,506 recalls

Medical DeviceJune 23, 2023· Datascope Corp.

Recalled Item: SENSATION PLUS 7.5Fr IAB Recalled by Datascope Corp. Due to During IAB...

The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2023· Datascope Corp.

Recalled Item: TRANS-RAY IAB Recalled by Datascope Corp. Due to During IAB catheter...

The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2023· Datascope Corp.

Recalled Item: MEGA 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...

The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2023· Datascope Corp.

Recalled Item: REINFORCED INTRODUCER SET Recalled by Datascope Corp. Due to During IAB...

The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2023· Datascope Corp.

Recalled Item: MEGA 8Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...

The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2023· Datascope Corp.

Recalled Item: SENSATION PLUS 8Fr. IAB Recalled by Datascope Corp. Due to During IAB...

The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2023· ALEMBIC PHARMACEUTICALS, INC.

Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by ALEMBIC PHARMACEUTICALS,...

The Issue: Defective Delivery System

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2023· Jost Chemical Co

Recalled Item: Zinc Sulfate Monohydrate Recalled by Jost Chemical Co Due to Zinc Sulfate...

The Issue: Zinc Sulfate Monohydrate, USP may contain elevated levels of lead.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2023· Trinidad Benham Corp

Recalled Item: GARBANZO BEANS Recalled by Trinidad Benham Corp Due to This recall has been...

The Issue: This recall has been initiated due to detection of glyphosate residues above...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 22, 2023· Canon Medical System, USA, INC.

Recalled Item: INFX-8000C XGCP-930AA TABLE SIDE CONSOLE Recalled by Canon Medical System,...

The Issue: The C-arm, used to set the position and angle of the x-ray exposure field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2023· Scican Ltd.

Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...

The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2023· Creganna Medical Devices

Recalled Item: Gore Tips Set Device Recalled by Creganna Medical Devices Due to Three lots...

The Issue: Three lots of product may be labeled with an incorrect expiration day

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2023· Scican Ltd.

Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...

The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...

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

Class II — Potential Health HazardOngoing
DrugJune 21, 2023· Dr Reddy's Laboratories Limited

Recalled Item: Tizanidine Tablets USP Recalled by Dr Reddy's Laboratories Limited Due to...

The Issue: Failed dissolution specification: Out of specification results observed in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2023· Scenic Fruit Company, LLC

Recalled Item: Trader Joe s Organic Tropical Fruit Blend Pineapple Recalled by Scenic Fruit...

The Issue: Potential for contamination with Listeria monocytogenes. Pineapples are...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 21, 2023· Scenic Fruit Company, LLC

Recalled Item: Cadia - Organic Pineapple Frozen Fruit Recalled by Scenic Fruit Company, LLC...

The Issue: Potential for contamination with Listeria monocytogenes. Pineapples are...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 21, 2023· Randox Laboratories Ltd.

Recalled Item: Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use...

The Issue: (1) There is vial to vial variation resulting in some vials recovering...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2023· Stryker Sustainability Solutions

Recalled Item: HoverMatt Recalled by Stryker Sustainability Solutions Due to 39-inche-wide...

The Issue: 39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2023· Beckman Coulter, Inc.

Recalled Item: Ringed DxI Reaction Vessels (RVs) Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter, Inc. is recalling Ringed DxI Reaction Vessels (RVs) as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS pheno-Angiography systems developed for single and biplane diagnostic...

The Issue: Due to a hardware issue in the cable connectors of the system generator, a...

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

Class II — Potential Health HazardOngoing