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. 2,624 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,624 in last 12 months

Showing 2744127460 of 51,768 recalls

Medical DeviceApril 13, 2018· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2018· AMA Wholesale

Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Recalled by...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 11, 2018· Seabear Company

Recalled Item: Cold Smoked Wild Coho Salmon Lox Recalled by Seabear Company Due to Mislabeling

The Issue: Products recalled due to water phase salt deviations and mislabeling of...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 11, 2018· Seabear Company

Recalled Item: Hot Smoked Keta Beergarden Salmon Recalled by Seabear Company Due to Mislabeling

The Issue: Products recalled due to water phase salt deviations and mislabeling of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 11, 2018· Stryker Neurovascular

Recalled Item: FlowGate2 Balloon Guide Catheter Recalled by Stryker Neurovascular Due to...

The Issue: There may be product manufactured with the outer diameter of the balloon...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: 4Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: 8Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Arrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R)...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing