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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,616 in last 12 months

Showing 70817100 of 13,355 recalls

DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: HEPARIN 1 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: fentaNYL 2 mcg/mL Recalled by Avella of Deer Valley, Inc. Store 38 Due to...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: NORepiNEPHrine 16 (NORepiNEPHrine Bitartrate (USP) 16 mg Recalled by Avella...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: 0.2% ROPivacaine - OnQ Pump Recalled by Avella of Deer Valley, Inc. Store 38...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: ePHEDrine 50mg Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 12, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 12, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 11, 2018· BioDiagnostic International

Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by BioDiagnostic...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2018· Qualgen, LLC

Recalled Item: TESTOSTERONE 200 mg PELLET Recalled by Qualgen, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.

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

Class III — Low RiskOngoing
Refund
DrugJune 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...

The Issue: Superpotent Drug: High out of specification assay value results for potency.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2018· Qualgen, LLC

Recalled Item: ESTRADIOL 20mg PELLET Recalled by Qualgen, LLC Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date.

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

Class III — Low RiskOngoing
Refund
DrugJune 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...

The Issue: Superpotent Drug: High out of specification assay value results for potency.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium Tc99m Medronate Recalled by...

The Issue: Lack of assurance of sterility: Technetium TC-99M Medronate Kit has a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2018· PharMEDium Services, LLC

Recalled Item: HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Recalled by...

The Issue: Superpotent and Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2018· HOSPIRA INC, LAKE FOREST

Recalled Item: Naloxone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST Due to...

The Issue: Presence of Particulate Matter; Potential for particulate matter on the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.45% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of assurance...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund