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. 2,824 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,824 in last 12 months

Showing 36413660 of 51,768 recalls

DrugDecember 23, 2024· Astellas Pharma US Inc.

Recalled Item: Prograf (tacrolimus) capsules Recalled by Astellas Pharma US Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2024· Astellas Pharma US Inc.

Recalled Item: Astagraf XL (tacrolimus extended-release capsules) 0.5 mg Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2024· First Aid Beauty Ltd

Recalled Item: First Aid Beauty Ultra Repair Cream Recalled by First Aid Beauty Ltd Due to...

The Issue: CGMP Deviations; product intended for quarantine was inadvertently distributed

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2024· Viatris Inc

Recalled Item: Cardura XL (doxazosin) extended release tablets 8 mg Recalled by Viatris Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2024· Viatris Inc

Recalled Item: Cardura XL (doxazosin) extended release tablets 4 mg Recalled by Viatris Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Oxoid Limited

Recalled Item: Lev5 Recalled by Oxoid Limited Due to Mislabeling

The Issue: Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Accuray Incorporated

Recalled Item: CyberKnife Treatment Delivery System Recalled by Accuray Incorporated Due to...

The Issue: Snap rings may become partially or completed detached from the shafts within...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ARTERIAL LINE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Certain lots Sterile Infusion Catheters which were mislabeled as having a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION Infusion Catheter Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Certain lots Sterile Infusion Catheters which were mislabeled as having a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Percussionaire Corporation

Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...

The Issue: Due to internal venturi component getting transiently stuck in the forward...

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

Class I — Serious Health HazardOngoing
DrugDecember 20, 2024· ENDO USA, Inc.

Recalled Item: Adrenalin Chloride Solution (Epinephrine Nasal Solution Recalled by ENDO...

The Issue: Labeling: Not Elsewhere Classified: misleading label similar in appearance...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 20, 2024· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to faulty circuit board in speed control remote use in conjunction with...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to faulty circuit board in speed control remote use in conjunction with...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

Recalled Item: PROLENE Polypropylene Suture Recalled by Ethicon, LLC Due to Sutures may...

The Issue: Sutures may have an open seal on the primary packaging, due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

Recalled Item: ETHIBOND EXCEL Polyester Suture Recalled by Ethicon, LLC Due to Sutures may...

The Issue: Sutures may have an open seal on the primary packaging, due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

Recalled Item: PERMA-HAND Silk Suture Recalled by Ethicon, LLC Due to Sutures may have an...

The Issue: Sutures may have an open seal on the primary packaging, due to a...

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

Class II — Potential Health HazardOngoing