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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 40701–40720 of 47,654 recalls
Recalled Item: Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix" LP with Echo PS" 6 x8 Reorder Number: 0144680 Indicated Recalled...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6" CircleReorder Number: Recalled...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Recalled by Davol,...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Recalled by Mar Cor Purification Due to Mar Cor...
The Issue: Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...
The Issue: Defective Delivery System; defective valve
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...
The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...
The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...
The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...
The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery MR450 Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....
The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.