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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,552 in last 12 months

Showing 1698117000 of 47,654 recalls

Medical DeviceOctober 7, 2020· Steris Corporation

Recalled Item: Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning...

The Issue: Potential for cleaning solution intrusion into endoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2020· Arjohuntleigh Magog, Inc.

Recalled Item: Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used Recalled by...

The Issue: Risk of Sling Clip breakage while in use with obsolete Flat Dynamic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgG Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: The cross-reactivity of the device may present an increased level of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Recalled by Becton,...

The Issue: Recent product complaints showing an unexpected cell population exhibiting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Bayer Medical Care, Inc.

Recalled Item: Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic...

The Issue: Specific lots of MEDRAD Stellant FLEX 150 mL syringe kits may have holes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Micro-Tech Usa

Recalled Item: Elastic Traction Device Recalled by Micro-Tech Usa Due to FDA has informed...

The Issue: FDA has informed Micro-Tech that the Elastic Traction Device is not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 2, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Candesartan Cilexetil and Hydrochlorothiazide Tablets Recalled by Mylan...

The Issue: Out-of-specification organic impurity results obtained during routine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodOctober 2, 2020· Seneca Foods Corporation

Recalled Item: Cinnamon Apple Crisps packaged under the following Brands and sizes:...

The Issue: Product may be contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 1, 2020· Desert Premium Group, LLC

Recalled Item: Trader Joe's Hatch Valley Salsa Recalled by Desert Premium Group, LLC Due to...

The Issue: One batch of salsa had a recorded equilibrium pH of 6.65.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...

The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...

The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...

The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...

The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...

The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...

The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing