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 21721–21740 of 47,654 recalls
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterStim(TM) System Recalled by Medtronic Neuromodulation Due to There is a...
The Issue: There is a potential for an unexpected increase in stimulation during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntraClude Intra-Aortic Occlusion Device Recalled by Edwards Lifesciences,...
The Issue: Possibility of balloon rupture in intra-aortic occlusion devices. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...
The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...
The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST- Amber Part/Catalog Number: 365978 Recalled by Becton...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST Part/Catalog No.365967 Recalled by Becton Dickinson &...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promacta (eltrombopag) 12.5 mg for Oral Suspension Recalled by Novartis...
The Issue: Cross Contamination with Other Products: product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol) Recalled by...
The Issue: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cadence Science Pressure Control Glass Syringe Recalled by Cadence Science,...
The Issue: The glass syringe used with Pressure Control Syringes may potentially break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.