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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 46261–46280 of 47,654 recalls
Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.075 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Topiramate Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Label Mix-Up: A typographical error in the product form on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OYSTER MEAT IQF TINY 40/8OZ PRODUCT OF KOREA Recalled by Icrest...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OYSTER MEAT IQF 6/5# LBS KR PRODUCT OF KOREA Recalled by Icrest...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand name is Yatta. OYSTERS 1/2 SHELL 144CT Recalled by Icrest...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OYSTER MEAT IQF LARGE 5/4 LBS PRODUCT OF KOREA Recalled by Icrest...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...
The Issue: There is a possibility that the screw channel that holds the rod in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...
The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OFIRMEV (acetaminophen) injection Recalled by Cadence Pharmaceuticals Due to...
The Issue: Presence of Particulate Matter: The firm initiated the recall due to visible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...
The Issue: A component within the handle of the Expedium Offset Torque Wrench is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...
The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercaptopurine Tablets Recalled by American Health Packaging Due to Failed...
The Issue: Failed USP Dissolution Test Requirements: This sub-recall is in response to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.