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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45081–45100 of 47,654 recalls
Recalled Item: Spice Cake Mix Recalled by Jiffy Food Service, LLC Due to Undeclared Allergen
The Issue: Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Inspira AIR Balloon Dilation system. Size 14 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 10 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 12 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 16 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 7 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Grip which is part of the Synthes Universal Nail Recalled by...
The Issue: Synthes is initiating a voluntary recall of the Flexible Grip (Part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...
The Issue: The Dens Instrument Set has been designed to facilitate the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Combination Clamp/Large External Fixation System Recalled by Synthes...
The Issue: The L1 hex nuts, used to tighten the Large Combination Clamp, were oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left)...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Recalled by Synthes USA HQ, Inc. Due to It...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GHH51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.