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. 2,711 recalls have been distributed to Washington in the last 12 months.
Showing 20981–21000 of 51,768 recalls
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...
The Issue: During the firm's review of May 2019 complaint data, a significant increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...
The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taspen's Organics Respiratory Tea Recalled by Green Water, LLC Due to The...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement Recalled...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...
The Issue: Sterile packaging incomplete seals may compromise sterility of the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.