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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16101–16120 of 47,654 recalls
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone Tablets Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cisatracurium Besylate Injection Recalled by Meitheal Pharmaceuticals Inc...
The Issue: Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TECNIS Toric 1-Piece IOL Recalled by Johnson & Johnson Surgical Vision Inc...
The Issue: Due to the release of nonconforming Intraocular Lenses (IOLs).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis / Sensis Vibe systems with software version VD12 and Recalled by...
The Issue: System may sporadically freeze (lock-up) during operation or while being in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gram-Negative Bacteria And Associated Resistance Markers Recalled by BioFire...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to The firm has...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O Organics Plant Based Mushroom and Veggie Organic Burger Patties Recalled...
The Issue: Labeling error caused product to claim Gluten Free and Vegan when it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Wildtree***Leslies Chili Blend***Organic & Gluten Free***Net Wt. 3.7 oz....
The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Wildtree***Taco Seasoning***Organic & Gluten Free***Net Wt. 8...
The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...
The Issue: Product was compromised during shipment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...
The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...
The Issue: Superpotent Drug. Lidocaine higher concentration than listed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.