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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.
Showing 26481–26500 of 47,654 recalls
Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...
The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fit & Active Chocolatey Chip Protein Meal Bars Recalled by Leclerc Foods USA...
The Issue: Firm received reports of flexible pieces of yellow plastic found in Fit &...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...
The Issue: It was discovered that the product units it imported may, at peak levels,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...
The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Teva...
The Issue: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...
The Issue: When calculating electron Monte Carlo dose with a very large number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...
The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDAN Telemetry Transmitter Recalled by Edan Diagnostics Due to Firm became...
The Issue: Firm became aware that it distributed 7 units in the U.S. that included a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Pump Recalled by CareFusion 303, Inc. Due to The syringe plunger...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to The syringe...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 6 Recalled by KRS Global Biotechnology, Inc Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzocaine 20% Recalled by KRS Global Biotechnology, Inc Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Savinase 100 mcg/mL Topical Solution Recalled by KRS Global Biotechnology,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chloramphenicol 50 mg/ Sulfamethoxazole 50 mg/ Amphotericin-B 5 mg capsules...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.