Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22761–22780 of 47,654 recalls
Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC20 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC50 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilling COOLEY SUMP-SUCTION TUBE Recalled by Teleflex Medical Due to The...
The Issue: The internal tip is missing from the device, causing the device to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLTOP HEARTH SELF RISE FLR 25LB and 50LB Recalled by Ardent Mills, LLC Due...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARDENT H&R SR FLR Recalled by Ardent Mills, LLC Due to Potential Salmonella...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MEMBERS MARK SELF RISE FLR 25LB Recalled by Ardent Mills, LLC Due to...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB Recalled by Ardent Mills, LLC...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.