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. 2,622 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,622 in last 12 months

Showing 64416460 of 27,451 recalls

Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Reusable Program - Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 5in Cath Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Valve Repair Kit Recalled by Merit Medical Systems, Inc. Due to There...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2023· Masimo Corporation

Recalled Item: Masimo LNCS TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...

The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2023· Masimo Corporation

Recalled Item: Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor Recalled by Masimo...

The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2023· Masimo Corporation

Recalled Item: Masimo LNCS TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...

The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2023· Masimo Corporation

Recalled Item: Masimo LNOP TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...

The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2023· Philips North America

Recalled Item: Patient Information Center iX Recalled by Philips North America Due to...

The Issue: During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic...

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

Class II — Potential Health HazardOngoing