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. 2,893 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,893 in last 12 months

Showing 1824118260 of 30,923 recalls

Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 24202 ADULT ECC Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2017· Teleflex Medical

Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...

The Issue: Teleflex is recalling these products because the jaws of the tool tip may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2017· Bioseal Corporation

Recalled Item: Custom surgical kits labeled as follows: (a) Suture Removal Set Recalled by...

The Issue: Custom surgical kits contain Aplicare Providone Iodine Prep Pads which were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet Recalled by Arrow International...

The Issue: The kit may contain an incorrect catheter component. Kits that should...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Siemens Healthcare Diagnostics

Recalled Item: BC Thrombin Reagent Kit Lot Number 46751 Recalled by Siemens Healthcare...

The Issue: The BC Thrombin Reagent kit lot 46751 (contains Thrombin Reagent lot 517468)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Arrow Multi Lumen CVC Kit (Central venous catheter) Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(TM) Normothermia System Recalled by 3M Company - Health Care...

The Issue: During a recent investigation, 3M confirmed that a programming translation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...

The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· C.R. Bard, Inc.

Recalled Item: Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch...

The Issue: Hydrogel peeling from the pads.

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

Class II — Potential Health HazardOngoing