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. 2,635 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5041–5060 of 47,654 recalls
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody Recalled by...
The Issue: Their is a potential for high background and off-target staining when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management Systems Recalled by Medivance Inc. Due to...
The Issue: If temperature management system fails to reach correct target water...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...
The Issue: Some lots of Capio SLIM do not consistently catch the suture after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...
The Issue: Some lots of Capio SLIM do not consistently catch the suture after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SymphoKnee Patella Sizing Template Recalled by LINK BIO CORP Due to The...
The Issue: The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infla-650 Herbal Dietary Supplement Recalled by Guru Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevelamer Carbonate for Oral Suspension 0.8g packets Recalled by Dr. Reddy's...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules Recalled...
The Issue: CGMP Deviations: Out of specification for dissolution
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blemfree All Day Lotion (salicylic acid 0.5% w/w) Recalled by Equibal Inc...
The Issue: CGMP Deviations: Manufactured without following Current Good Manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Budesonide Recalled by Medisca Inc. Due to CGMP Deviations and Presence of...
The Issue: CGMP Deviations and Presence of Particulate Matter: Glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...
The Issue: A potential issue with ARTIS icono systems equipped with a small detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...
The Issue: A potential issue with ARTIS icono systems equipped with a small detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...
The Issue: A potential issue with ARTIS icono systems equipped with a small detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Amerisource Health...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...
The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...
The Issue: The tube may fall into the surgical site during the grasping process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.