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. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1610116120 of 51,768 recalls

Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Recalled by...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Arrow International Inc

Recalled Item: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm Recalled...

The Issue: Marketed without a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Arrow International Inc

Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr....

The Issue: Marketed without a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Arrow International Inc

Recalled Item: Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm Recalled by Arrow...

The Issue: Marketed without a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Arrow International Inc

Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr....

The Issue: Marketed without a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Bard Access Systems Inc.

Recalled Item: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard...

The Issue: Catheter convenience kits contain the incorrect guidewire. Kits were labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Vero Biotech, LLC

Recalled Item: GENOSYL DS Recalled by Vero Biotech, LLC Due to Reports received of NO...

The Issue: Reports received of NO measured below desired dose during transition between...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 19, 2021· Smith & Nephew, Inc.

Recalled Item: LEGION Posterior Stabilized OXINIUM Femoral Component Recalled by Smith &...

The Issue: The device components experienced a manufacturing process error that...

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

Class II — Potential Health HazardOngoing
DrugMay 18, 2021· Miracle 8989

Recalled Item: PremierZEN Platinum 8000 capsule Recalled by Miracle 8989 Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 18, 2021· Miracle 8989

Recalled Item: maXXzen Platinum 12000 capsule Recalled by Miracle 8989 Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 18, 2021· Miracle 8989

Recalled Item: PremierZEN Gold 7000 capsule Recalled by Miracle 8989 Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 18, 2021· Torn Ranch LLC.

Recalled Item: Torn Ranch Organic Dark Chocolate Blueberries 18oz. resealable bags Recalled...

The Issue: Recalling one lot code of Torn Ranch Organic Dark Chocolate Blueberries 18...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 18, 2021· Stryker Spine

Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...

The Issue: The products experienced a 12-hour excursion from the required temperature...

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

Class II — Potential Health HazardOngoing