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 41661–41680 of 47,654 recalls
Recalled Item: Integrity. Version 1.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....
The Issue: Potential collision risk when using XVI and external beam shaping devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RTP System. Used to create treatment plans for any Recalled by Elekta,...
The Issue: When bolus is present, the Effective Depth (with bolus) to the weight point...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...
The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HT Connect Peripheral Guide Wire Part Number Description 1012587 018...
The Issue: Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...
The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe's Authentically Korean Seaweed Salad with Spicy Dressing Recalled...
The Issue: Jayone Foods is recalling Trader Joe's Dried Seaweed Salad with Spicy...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dr. Sheffield Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FAMILY wellness Triple Antibiotic Ointment. NET WT 1 OZ (28 g) Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dollar General Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senor Murphy Santa Fe Candymaker Peanut Brittle Recalled by Senor Murphy...
The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Senor Murphy Santa Fe Candymaker Pinon Brittle Recalled by Senor Murphy...
The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Senor Murphy Santa Fe Candymaker Cashew Crunch Recalled by Senor Murphy...
The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Senor Murphy Santa Fe Candymaker Pecan Bueno Recalled by Senor Murphy...
The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme...
The Issue: Dietary Supplements were made with bulk products provided by National Enzyme...
Recommended Action: Do not consume. Return to store for a refund or discard.