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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3241–3260 of 47,654 recalls
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO...
The Issue: Due to an error message that prevents users from utilizing carboxyhemoglobin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 35 ECG cable Recalled by Physio-Control, Inc. Due to Product shipped...
The Issue: Product shipped with incorrect IFU. IFU does not include proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Control Panel...
The Issue: Internal quality control procedures were not followed correctly for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel...
The Issue: Internal quality control procedures were not followed correctly for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BADGER 50 Recalled by The W.S. Badger Company, Inc. Due to Labeling: Missing...
The Issue: Labeling: Missing Label: The finished product potentially missing the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Inflectra (infliximab-dyyb) Recalled by McKesson Due to cGMP Deviations:...
The Issue: cGMP Deviations: Product intended for quarantine was inadvertently distributed.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: HOMEDICS Product Name: Air Compression Leg Massager...
The Issue: Regulatory documentation error and misleading color packaging claim.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M V.A.C. VIA Negative Pressure Wound Therapy System /US Recalled by KCI...
The Issue: Due to increase in complaints related to leak alarms
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Prevena Plus 125 Therapy Unit and System Kits by KCI USA, INC. Due to Due...
The Issue: Due to increase in complaints related to leak alarms
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Front Panel: Shirakiku brand Recalled by Wismettac Asian Foods, Inc. Due to...
The Issue: Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Recommended Action: Do not consume. Return to store for a refund or discard.