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. 1,965 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,965 in last 12 months

Showing 1846118480 of 29,208 recalls

Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Cook Inc.

Recalled Item: Cook Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Correction...

The Issue: Correction to the product Instructions for Use because the current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Durability characteristics of reusable instruments were not established

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: When cut lines are shown on an image, the lines may go from being vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Merge PACS did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Estrogen Receptor (EP1) 7.0 mL Catalog number 249R-28 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Her2/Neu (EP3) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Innovasis, Inc

Recalled Item: Opteryx Variable Rescue Screw Recalled by Innovasis, Inc Due to Opteryx...

The Issue: Opteryx Variable Rescue Screws are engraved with incorrect (larger) size (16...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· GE Healthcare, LLC

Recalled Item: Infant Warmer System (IWS) Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: CD117 Recalled by Cell Marque Corporation Due to Cell Marque has determined...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Adenovirus (20/11 & 2/6) Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing