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.
Showing 6781–6800 of 27,451 recalls
Recalled Item: Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N)...
The Issue: An increased incidence of damage to the nut band from a new vendor (Boamax)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)...
The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens...
The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Easy Read App associated with First Response Pregnancy Test Sticks Recalled...
The Issue: Church & Dwight First Response Pregnancy Kits was marketed with the Easy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Black Intelligent Reload Recalled by Covidien, LP Due to...
The Issue: Affected lots have the potential for a broken sled vane, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator System Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to There...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a Recalled...
The Issue: An observed trend of high conductivity dialysate alarms in a hemodialysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Side Cart Recalled by Intuitive Surgical, Inc. Due to Preventative...
The Issue: Preventative maintenance data was used to identify instrument Arms, part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network...
The Issue: Infusion pump PCs with specific software/network cards/IP addresses can have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Large component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Medium component of VS Newborn Recalled by SUREPULSE...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Small component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.