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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 42081–42100 of 47,654 recalls
Recalled Item: GL Completia Recalled by Schwabe North America, Inc. Due to Nature's Way...
The Issue: Nature's Way (NW) is voluntary recalling a number of products because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Way Recalled by Schwabe North America, Inc. Due to Nature's Way...
The Issue: Nature's Way (NW) is voluntary recalling a number of products because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Way Recalled by Schwabe North America, Inc. Due to Nature's Way...
The Issue: Nature's Way (NW) is voluntary recalling a number of products because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NL C 24/7 Bulk Caps Recalled by Schwabe North America, Inc. Due to Nature's...
The Issue: Nature's Way (NW) is voluntary recalling a number of products because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Flex Recalled by New Algae Company Due to Flex dietary supplement product is...
The Issue: Flex dietary supplement product is recalled because the finished label does...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EDGE Recalled by New Algae Company Due to EDGE dietary supplement product is...
The Issue: EDGE dietary supplement product is recalled because the finished label does...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...
The Issue: It was discovered the CT portion of the scan was interrupted ( stopping the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any...
The Issue: A safety risk regarding a potentially existing dark current radiation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS brand ONCOR series Linear Accelerator Linac systems with component:...
The Issue: A safety risk regarding a potentially existing dark current radiation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette...
The Issue: Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...
The Issue: It was reported that the siderail may appear latched when it is not, due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns" Venous Return Cannulae Recalled by Terumo Cardiovascular Systems...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns" Soft-Flow¿ Aortic Cannula without Suture Flange Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Capsules Recalled by Sandoz Incorporated Due to Cross...
The Issue: Cross Contamination with Other Products: findings of carryover of trace...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.