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. 2,464 recalls have been distributed to District of Columbia in the last 12 months.
Showing 21841–21860 of 27,451 recalls
Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...
The Issue: A wire component on the distal grasping assembly of the device became detached..
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS ROC Crown Component 4UR (5/pk) Recalled by Specialty Appliance Works,...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialty MiniScope Mech. Set Size 18 Recalled by Specialty Appliance Works,...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Recalled by Specialty...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit Recalled by Specialty Appliance...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 Recalled by Specialty...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HTM Mechanism Set Set 16 Recalled by Specialty Appliance Works, Inc. Due to...
The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.