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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,639 in last 12 months

Showing 39213940 of 47,654 recalls

DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: ABSORBINE JR PAIN RELIEVING KNEE PATCH Recalled by Unexo Life Sciences...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: HealthWise PERIOD PATCH Menstrual Pain Relief Recalled by Unexo Life...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2024· GE Healthcare (China) Co., Ltd.

Recalled Item: GE Proteus XR/A radiographic system Recalled by GE Healthcare (China) Co.,...

The Issue: Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by...

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Ramipril Capsules USP 10 mg Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Active pharmaceutical ingredient was sourced from an...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Ramipril Capsules USP 2.5 mg Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Active pharmaceutical ingredient was sourced from an...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Ramipril Capsules USP 5 mg Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Active pharmaceutical ingredient was sourced from an...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2024· Cipla USA, Inc.

Recalled Item: Lanthanum Carbonate Chewable Tablets Recalled by Cipla USA, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Complaints received of crushed and...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2024· Cipla USA, Inc.

Recalled Item: Lanthanum Carbonate Chewable Tablets Recalled by Cipla USA, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Complaints received of crushed and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 23, 2024· Micro-X Ltd.

Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to During...

The Issue: During internal testing it was found that if the system is Ready to expose...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Lab Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE COLLECTION VHC Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clean Catch Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE KIT W/BD CUP Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: UA KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINALYSIS KIT 4 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
DrugOctober 22, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Morphine Sulfate Extended-Release Tablets 15 mg Recalled by Dr. Reddy's...

The Issue: Failed Impurities/Degradation Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Morphine Sulfate Extended-Release Tablets 30 mg Recalled by Dr. Reddy's...

The Issue: Failed Impurities/Degradation Specification

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 22, 2024· ICU Medical, Inc.

Recalled Item: Allegedly counterfeit batteries manufactured by CSB batteries being used...

The Issue: ICU Medical has received reports of allegedly counterfeit CSB batteries...

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

Class I — Serious Health HazardOngoing