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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.
Showing 44981–45000 of 47,654 recalls
Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and...
The Issue: The firm has received numerous complaints of the cannulated screw driver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Logic Comprehensive Knee Prosthesis System Recalled by Exactech,...
The Issue: A dimensional mismatch was identified which can potentially allow for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Firebird Spinal Fixation System Recalled by Orthofix, Inc Due to There is a...
The Issue: There is a possibility that the Set Screw (p/n 90-2923) sub-component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Safety Blood Collection Set + Luer Adapter Recalled by Greiner...
The Issue: The VACUETTE Safety Blood Collection Set + Luer Adapter may display leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vistide (cidofovir) Injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: Particulate matter was found in some vials...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Suprax (cefixime for oral suspension) USP Recalled by Lupin Pharmaceuticals...
The Issue: Discoloration; Product may not meet specifications for color description...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus...
The Issue: During the course of product monitoring, Siemens became aware of a tolerance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echelon Recalled by Hitachi Medical Systems America Inc Due to Hitachi...
The Issue: Hitachi discovered a software error that can occur when simultaneously...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic...
The Issue: Potential failure of the braking system that controls the O-arm Imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lansoprazole Delayed-release Capsules Recalled by Mylan Pharmaceuticals Inc....
The Issue: Presence of Foreign Tablets/Capsules: Bottles of lansoprazole 30 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Z Pro 25 High Protein Supplement Net. Wt. 1.3 oz. Recalled by R-Kane...
The Issue: Z Pro High Protein Vanilla Flavor Supplement is under recall because it...
Recommended Action: Do not consume. Return to store for a refund or discard.