Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,798 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,798 in last 12 months

Showing 82618280 of 51,768 recalls

DrugSeptember 8, 2023· Novartis Pharmaceuticals Corp.

Recalled Item: SANDIMMUNE Oral Solution (cyclosporine oral solution Recalled by Novartis...

The Issue: Crystallization: bottles of Sandimmune Oral Solution were determined to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Centricity Universal Viewer Workflow Manager Recalled by GE Healthcare Due...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Medical Systems China Co., Ltd.

Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...

The Issue: There is a potential interruption of data communication between E-modules...

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

Class II — Potential Health HazardOngoing
DrugSeptember 7, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent: Out of Specification result observed for low assay

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 7, 2023· Blue Belt Technologies, Inc

Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...

The Issue: CORI software was missing a planning stage that appears in cases of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Encore Medical, LP

Recalled Item: RSP Glenoid Baseplate Recalled by Encore Medical, LP Due to Coating hex did...

The Issue: Coating hex did not engage with the Straight Mod Hexdriver or with the Hex...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Beckman Coulter Biomedical Division

Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...

The Issue: The firm has identified that the Transferrin reagent does not meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 Recalled by...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000 Recalled by...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R ()...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings,...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T GEN 2 Bibag without CDX Recalled by Fresenius Medical Care Holdings,...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing