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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 31001–31020 of 47,654 recalls
Recalled Item: Heater Cooler Unit Usage: The Heater-Cooler Unit (HCU 30) supplies Recalled...
The Issue: There is the potential for contaminated water to enter parts of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator is...
The Issue: Oxygen tubing and the oxygen connector of the Hamilton-MR1 could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GoPicnic Turkey Slices & Cheddar Cheese Recalled by SSI-GoPicnic LLC Due to...
The Issue: Bagel chips containing wheat gluten included in a meal labeled "gluten free."
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Label reads in part "*** Bob's Red Mill *** PREMIUM Recalled by Bob's Red...
The Issue: The firm is voluntarily recalling one lot of Guar Gum due to due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: On the Border Cafe Style Tortilla Chips 18 oz. and Recalled by Truco...
The Issue: Possible metal fragments in corn flour.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: On the Border Blue Corn Tortilla Chips 7.25 oz. and Recalled by Truco...
The Issue: Possible metal fragments in corn flour.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OEC Brivo 715 Prime Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC Brivo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold Kit. Catalog Number K09-11867AP Recalled by Merit Medical Systems,...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluid Management Set. Catalog Number K08-MP5159A Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waste Management Kit. Catalog Number K10-04381AP Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V. Mueller Neuro/Spine Recalled by Cardinal Health 200, LLC Due to Potential...
The Issue: Potential risk associated with corrosion demonstrated on the distraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product...
The Issue: There is a potential for a component failure of the device which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog...
The Issue: O-arm O2 Surgical Imaging System Spatial calibration may be erroneous in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARICALCITOL Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARICALCITOL Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARICALCITOL Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cookies Bergen Recalled by Dollar General Corporation Due to Mold found in...
The Issue: Mold found in cookie product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CD79b PE (ASR) Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: CD79b (SN8) PE is contaminated with a FITC conjugate of unknown antigenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.