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. 2,529 recalls have been distributed to District of Columbia in the last 12 months.
Showing 19161–19180 of 47,654 recalls
Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...
The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...
The Issue: Potential for the expiration date on the outer label that was applied by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Tablets Recalled by Denton Pharma, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Tablets Recalled by Denton Pharma, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIPO B 25MG/50MG/50MG/1000MCG/ML (10ML VIAL) in 20 mL syringe and Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BAC 160MCG/HYDROM 16MG/ML INJ in 20 mL syringe Assurance Infusion Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 10MG/ FENT 1000MCG/ML INJ in 20 mL syringe Assurance Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROMORPHONE 2MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROM 1MG/MORP 20MG/SUF 100MCG/ML INJ in 20 mL syringe Assurance Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BAC 2400MCG/ FENT 2600MCG/ MORP 3600MCG/ML INJ in 20 mL Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 5.3MG/ FENT 1050 MCG/ML INJ in 20 mL syringe Recalled by Assurance...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.