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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 42501–42520 of 47,654 recalls
Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...
The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Body Oil)...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Scalp Oil)...
The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PGE-1 Recalled by University Compounding Pharmacy Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: University Compounding Pharmacy is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution Recalled by Altaire...
The Issue: Non-Sterility: Customer complaints of mold in the product after use and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PGE-1 Recalled by University Compounding Pharmacy Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: University Compounding Pharmacy is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate (Sesame Oil) 200mg/mL Injection Recalled by...
The Issue: Lack of Assurance of Sterility: University Compounding Pharmacy is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Concentrated Motrin (ibuprofen) Infants' Drops Oral Suspension Recalled by...
The Issue: Presence of Foreign Substance: process-related particulates which may be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate/Testosterone Propionate 180-20 mg/mL Injection...
The Issue: Lack of Assurance of Sterility: University Compounding Pharmacy is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.