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. 2,773 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,773 in last 12 months

Showing 1328113300 of 51,768 recalls

Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC...

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: 11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (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: 11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1...

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: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0...

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: 11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)...

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: 11278V 11278VK CMOS Video Ureteroscope Z17744US-A (04/2016) Recalled by Karl...

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
DrugMarch 31, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2022· MERCK SHARP & DOHME CORP

Recalled Item: Janumet (sitagliptin and metformin HCl) tablets Recalled by MERCK SHARP &...

The Issue: Presence of foreign substance: Presence of stainless steel particulates in...

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

Class II — Potential Health HazardOngoing
Refund
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 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· 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· 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
DrugMarch 30, 2022· Unilever United States Inc.

Recalled Item: Suave 24-Hour Protection Aerosol Antiperspirant Powder scent Recalled by...

The Issue: Chemical contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund