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. 2,612 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,612 in last 12 months

Showing 1022110240 of 47,654 recalls

Medical DeviceJanuary 20, 2023· Coltene Whaledent Inc

Recalled Item: SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of...

The Issue: Screw connection between the turbine head and the push button may loosen and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 18, 2023· Mondelez Global Llc

Recalled Item: Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) Recalled by...

The Issue: Undeclared FD&C Yellow No. 5

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2023· Philips North America

Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due...

The Issue: The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 17, 2023· Urban Electric Power

Recalled Item: Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v Recalled by Urban...

The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2023· Urban Electric Power

Recalled Item: Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v) Recalled by Urban Electric...

The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2023· Fisher Scientific Co., LLC

Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...

The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2023· Fisher Scientific Co., LLC

Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...

The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2023· Fujifilm Irvine Scientific, Inc.

Recalled Item: Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) # 9305 Recalled...

The Issue: Due to the detection of oil toxicity in several lots of Oil for Embryo...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Hologic, Inc.

Recalled Item: Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D...

The Issue: C-Arm unexpected movement may cause blunt trauma should the tube arm impinge...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph mCT: a) Flow 64-4R Seismic Recalled by Siemens Medical...

The Issue: This is a potential problem with the locking mechanism that is used to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph Vision: a) 450 Recalled by Siemens Medical Solutions USA,...

The Issue: This is a potential problem with the locking mechanism that is used to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...

The Issue: This is a potential problem with the locking mechanism that is used to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 13, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by SUN...

The Issue: Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 13, 2023· Nephron Sc Inc

Recalled Item: S2 Racepinephrine Inhalation Solution Recalled by Nephron Sc Inc Due to...

The Issue: Short Fill

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 13, 2023· Nephron Sc Inc

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator (racephedrine...

The Issue: Short Fill

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2023· Accord Healthcare, Inc.

Recalled Item: Allopurinol Tablets USP Recalled by Accord Healthcare, Inc. Due to Presence...

The Issue: Presence of Foreign Substance: Presence of a small piece of green plastic...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2023· Nephron Sc Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Nephron Sc Inc Due to CGMP...

The Issue: CGMP Deviations: potential for trace amounts of product carryover.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2023· Nephron Sc Inc

Recalled Item: Sterile Water for Injection Recalled by Nephron Sc Inc Due to CGMP...

The Issue: CGMP Deviations: potential for trace amounts of product carryover.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2023· Ortho Molecular Products, Inc.

Recalled Item: Fiber Powder Recalled by Ortho Molecular Products, Inc. Due to Raw material...

The Issue: Raw material tested positive for Cronobacter sakazakii.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2023· Amerisource Health Services LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications: This recall is being initiated in support...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund