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. 1,145 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,145 in last 12 months

Showing 8301–8320 of 29,208 recalls

Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018) Recalled by...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· CELLTRION USA INC

Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...

The Issue: Point of Care (PoC) rapid test products were distributed to customers who...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge 9100-Series Washer Disinfector models: 9120E Recalled by Getinge Usa...

The Issue: Inadequate documentation verifying whether device installation has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2022· CooperSurgical, Inc.

Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...

The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2022· CooperSurgical, Inc.

Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...

The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...

The Issue: Forceps do not comply with Olympus standards for the amount of force...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2022· CooperSurgical, Inc.

Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...

The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· restor3d Inc.

Recalled Item: Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product...

The Issue: Product labeled incorrectly. The lot was labeled with Small footprint when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Devicor Medical Products Inc

Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...

The Issue: Small patient labels do not match the primary device label. The primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· restor3d Inc.

Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...

The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Neuromodulation

Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...

The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Neuromodulation

Recalled Item: Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with...

The Issue: The Implantable Neurostimulator Model may be susceptible to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Inc

Recalled Item: Instructions for Use Recalled by Medtronic Inc Due to Errors and...

The Issue: Errors and inconsistencies that were identified in the Instruction for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Howmedica Osteonics Corp.

Recalled Item: Triathlon Tritanium Tibial Component (Size 6) Recalled by Howmedica...

The Issue: Stryker has discovered a potential product mix where the size of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Abbott Vascular

Recalled Item: Dragonfly OpStar Imaging Catheter Recalled by Abbott Vascular Due to There...

The Issue: There is a potential that the proximal marker may separate from the imaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2022· Accriva Diagnostics, Inc.

Recalled Item: The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 Recalled by...

The Issue: Two whole blood Platelet Reactivity tests exist that share the same reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· restor3d Inc.

Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...

The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...

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

Class II — Potential Health HazardOngoing