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. 2,640 recalls have been distributed to Washington in the last 12 months.
Showing 25441–25460 of 51,768 recalls
Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...
The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...
The Issue: One lot of the specified needles is not performing as intended due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...
The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Recalled by...
The Issue: ParaPost Plus Titanium Posts contain stainless steel post that are a size 4
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to The...
The Issue: The catheter failed the endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrochlorothiazide Tablets USP Recalled by Accord Healthcare, Inc. Due to...
The Issue: Product Mix-Up: customer complaint that a sealed bottle labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methyl-Cobalamin injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Mayne Pharma Inc Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.