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. 1,713 recalls have been distributed to District of Columbia in the last 12 months.
Showing 40701–40720 of 47,654 recalls
Recalled Item: TUMOR RESECTION KIT 9733607 NON-INVASIVE Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAG 9732315 MOUSE STERILE 15 PK Recalled by Medtronic Navigation, Inc. Due...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHUNT KIT 9733605 NON-INVASIVE Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATIENT TRACKER 9733534XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT TRACKER 9733533XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP 9730950 STRL SPHERE Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPSY NEEDLE KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems Model 610 Washer/High Level Disinfector. Maximum weight of...
The Issue: Cenorin LLC is voluntarily recalling HLD Systems Model 610 Washer/High Level...
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: 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: 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: 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: 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: 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: 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: 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.