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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,584 in last 12 months

Showing 1254112560 of 47,654 recalls

Medical DeviceApril 19, 2022· Haemonetics Corporation

Recalled Item: Product Name: TEG5000 Analyzer (07-022 Recalled by Haemonetics Corporation...

The Issue: When the TEG 5000 Analyzer including TEG Analytical Software is used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2022· Smith & Nephew Inc

Recalled Item: LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 Recalled...

The Issue: It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box...

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

Class II — Potential Health HazardOngoing
FoodApril 18, 2022· World Variety Produce Inc dba Melissa's

Recalled Item: Organic Marketside Zucchini 2 Count packages/8 per case Ingredients: Organic...

The Issue: Product may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 18, 2022· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Models: 3500 Recalled by Smiths Medical ASD Inc. Due...

The Issue: Multiple issues with the potential for interruption of therapy or...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2022· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Model: Model 4000-0100-50 Recalled by Smiths Medical...

The Issue: Multiple issues with the potential for interruption of therapy or...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2022· GE Healthcare, LLC

Recalled Item: Replacement back up batteries distributed on or after April 1 Recalled by GE...

The Issue: Insufficient battery backup power resulting in premature shutdown of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2022· GE Healthcare, LLC

Recalled Item: Back up batteries in Ventilators labeled as the following: a. Recalled by GE...

The Issue: Insufficient battery backup power resulting in premature shutdown of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2022· ProgenaCare

Recalled Item: progenamatrix Human Keratin Matrix Recalled by ProgenaCare Due to Inner...

The Issue: Inner pouch seal may be inadequate resulting in lack of sterility.

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

Class II — Potential Health HazardOngoing
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Akorn, Inc.

Recalled Item: Lidocaine Hydrochloride Oral Topical Solution Recalled by Akorn, Inc. Due to...

The Issue: Failed viscosity specification - product was below specificcation

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

Class III — Low RiskOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Lidocaine 2.5% and Prilocaine 2.5% Cream Recalled by Teva Pharmaceuticals...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2022· Driscoll's Inc.

Recalled Item: Driscoll's Blackberries (Fresh) 12x6 oz Recalled by Driscoll's Inc. Due to...

The Issue: California Department of Pesticide Regulation detected the presence of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 14, 2022· Turbett Surgical, Inc.

Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Devices...

The Issue: Devices were subject to unapproved rework processes.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2022· Medtronic Inc

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Medtronic Inc Due to The pump...

The Issue: The pump may have a welding defect that can lead the pump to malfunction....

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 14, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 ToRC IgM Reagent Pack Recalled by Bio-Rad Laboratories, Inc....

The Issue: Performance concerns for the CMV IgM analyte. Analyte has demonstrated...

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

Class II — Potential Health HazardOngoing