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. 2,591 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11161–11180 of 27,451 recalls
Recalled Item: Restore Clinician Programmer Application Software Recalled by Medtronic...
The Issue: The original version of the A71100 Restore Clinician Programmer Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Match Point System The Match Point System is intended to Recalled by...
The Issue: The procedure side indicated in the top header of the Shoulder Case Planning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98...
The Issue: A low risk of a false positive result being issued with a laboratory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-SARS-CoV-2 IgG Reagent Pack Recalled by Ortho Clinical...
The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Anti-SARS-CoV-2 Total Reagent Recalled by Ortho Clinical Diagnostics...
The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No:T-SPOT.TB8 Recalled by Oxford Immunotec Due to Incorrect expiration...
The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No:T-SPOT.TB50 Recalled by Oxford Immunotec Due to Incorrect...
The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system...
The Issue: 1) 1) Potential intermittent issue may cause image data problems, may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This Recalled by...
The Issue: 1) Service function problem may cause false marking of a bad channel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointts sistema de ellmlnact! Recalled by OraSure Technologies, Inc. Due to...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personelle OTC Skin Tag Remover Recalled by OraSure Technologies, Inc. Due...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Advanced Wart Remover Kit Recalled by OraSure Technologies, Inc. Due to...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SINGLES Carbide US-No. FG556 Recalled by Hager & Meisinger Gmbh Due to...
The Issue: US-dates between the product package label and the bar code display.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA Recalled by Qiagen...
The Issue: There is an increased rate of potential false positive results for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.