State

District of Columbia product recalls

73,381 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total: 2,798
Critical: 240
Severe: 1,083
Most recent: 2026-09-23

Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,083 (39%) are Severe.

Which agencies issued them

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19351–19375 of 76179

HighFDA (Devices)·Z-0093-2023·2022-10-26
Siemens N Antiserum to Human IgG Recall for High-Dose Performance Failure
Siemens Healthcare Diagnostics recalls N Antiserum to Human IgG reagent for laboratory analyzers because it does not meet expected High-Dose Hook Effect performance specifications for IgG measurements in certain sample types.
Product
N Antiserum to Human IgG, 2mL Variant for BN II System and BN ProSpec System-IVD Siemens Material Number (SMN): 10446297
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0015-2023·2022-10-26
Saline Solution Injection Recalled Nationwide Due to Sterility and Leakage
Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection distributed nationwide due to lack of assurance of sterility and potential leakage. Multiple lot numbers with expiration dates ranging from May 2023 to August 2023 are affected.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0091-2023·2022-10-26
IV Extension Sets Recalled for Bonded Joint Failure and Leakage Risk
B. Braun extension sets (Product Code 470169) are recalled due to high probability of bonded joint failure, which may cause leakage or detachment during use, risking bloodstream infections and medication exposure.
Product
Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per carton. A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood upon insertion of a male luer connector.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0064-2023·2022-10-26
Nestle Cookie Dough Recalled for Plastic Contamination
Nestle-USA is recalling Stuffed Chocolate Chip Cookie Dough due to consumer complaints of white plastic pieces found in the product. Consumers should not eat the product.
Product
"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"
Category
Food
Distribution
40 states
HighFDA (Food)·F-0069-2023·2022-10-26
Tastykake Glazed Cherry Pie Recalled Due to Undeclared Soy Lecithin
Flowers Foods is recalling Tastykake Glazed Cherry Pie due to undeclared soy lecithin in the product. The recalled product may pose a health risk to consumers with soy allergies.
Product
TASTYKAKE GLAZED CHERRY PIE NET WT 4.5 OZ (128g) UPC 0 25600 00969 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0098-2023·2022-10-26
Synthes Orthopedic Implant Drill Kit Recall: Incorrect Drill Guide Size
Synthes (USA) Products LLC is recalling 81 SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kits nationwide due to incorrect drill guide sizing. The defect could result in bone damage and incorrectly placed drill holes during orthopedic surgery.
Product
SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No. SE-2020-10. Used with DePuy Synthes SPEEDSHIFT Continuous Compression Staple Implants for bone fixation and management of fracture and reconstructive surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V805000·2022-10-26
Sunset Park & RV Recalls 2022 Sun Lite and Rush Travel Trailers
Sunset Park & RV is recalling 2022 Sun Lite and Rush travel trailers because a welded seam on the awning fabric may separate, causing the awning to drop unexpectedly.
Product
SUNSET PARK & RV — SUNSET PARK & RV SUNLITE, RUSH
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0065-2023·2022-10-26
Mrs. Freshley's Apple Fruit Pie recalled for undeclared soy allergen
Flowers Foods is recalling Mrs. Freshley's Apple Fruit Pie (4.5 oz) because some packages may contain undeclared soy lecithin, a major allergen. Consumers with soy allergies should not consume the affected product.
Product
Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0089-2023·2022-10-26
Dimension Vista HDLC Reagent Cartridge Recalled for Inaccurate Lab Results
Siemens is recalling 1,592 units of Dimension Vista HDLC reagent cartridges due to potential for erroneous test results. Affected cartridges may produce falsely high or low HDL cholesterol measurements.
Product
Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent cartridge, IVD Siemens Material Number (SMN): 10464340 Catalog Number: K3048A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0067-2023·2022-10-26
Tastykake Glazed Apple Pie Recalled for Undeclared Soy Allergen
Flowers Foods is recalling Tastykake Glazed Apple Pie because soy lecithin is not declared on the labels. People with soy allergies could be at risk.
Product
TASTYKAKE GLAZED APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 00972 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0107-2023·2022-10-26
Medicina ENFit enteral syringe recall due to material specification defect
Medicina is recalling ENFit 1ml enteral syringes because the plunger was manufactured with polyethylene instead of approved polypropylene. This material defect could affect plunger function and device safety.
Product
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0114-2023·2022-10-26
Medicina Reusable Oral Syringe recalled for incorrect plunger material
Medicina Uk Ltd is recalling Medicina Reusable Oral Syringe 2.5ml units because plunger components were manufactured with polyethylene instead of the specified polypropylene material.
Product
Medicina Reusable Oral syringe 2.5ml Code: OTH25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0111-2023·2022-10-26
Medicina Oral Tip Syringe recalled for unapproved plunger material
Medicina Uk Ltd is recalling Medicina Oral Tip Syringe 2.5ml nationwide because the plunger component was manufactured with polyethylene instead of the approved polypropylene material.
Product
Medicina Oral Tip Syringe 2.5ml Code: OT25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0070-2023·2022-10-26
Tastykake Glazed Lemon Pie Recalled for Undeclared Soy
Flowers Foods recalled Tastykake Glazed Lemon Pies due to undeclared soy lecithin in certain packages. Products with Enjoy By dates of Oct. 28, 31, Nov. 4, and 7 are affected.
Product
TASTYKAKE GLAZED LEMON FLAVORED PIE NET WT 4.5 OZ (128g) UPC 0 25600 00967 3 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0117-2023·2022-10-26
MitraClip G4 and TriClip G4 Cardiac Devices Recalled for Clip Locking Malfunction
Abbott has recalled MitraClip G4 and TriClip G4 cardiac repair devices due to clip locking malfunctions that may prevent proper device deployment. These malfunctions could lead to failed procedures and serious complications including device embolization.
Product
Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT, MitraClip G4 CDS NTW REPAIR-MR Clinical/CDS0704-NTW, MitraClip G4 CDS XT REPAIR-MR Clinical/CDS0704-XT, MitraClip G4 CDS XTW REPAIR-MR Clinical/CDS0704-XTW, TriClip NT Clip Delivery Sys CLIN/TCDS0203-NT…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0103-2023·2022-10-26
Optima Coil System Pouch Labels Do Not Match Carton Labels
BALT USA is recalling Optima Coil System models OPTI0208CSS10 and OPTI0308CSS10 due to a labeling discrepancy where pouch labels do not match carton labels. These endovascular devices require verification before use.
Product
Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0014-2023·2022-10-26
OTC Sinus Pressure and Pain Cough Product Mislabeled as Decongestant-Free
Walgreens Sinus Pressure, Pain & Cough tablets are mislabeled as 'Decongestant Free' but contain Phenylephrine HCl, a nasal decongestant. The labeling error affects 66,384 boxes distributed nationwide.
Product
SINUS PRESSURE, PAIN AND COUGH — SINUS PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0108-2023·2022-10-26
Medicina ENFit Enteral Syringes Recalled for Incorrect Plunger Material
Medicina Uk Ltd is recalling Medicina ENFit 5ml Reusable Enteral Syringes because the plunger component was manufactured with polyethylene instead of the specified polypropylene material.
Product
Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0010-2023·2022-10-26
FDA Recalls Flunisolide Nasal Solution Due to Out-of-Specification Impurities
Ingenus Pharmaceuticals is recalling Flunisolide Nasal Solution nationwide because the product contains impurities that exceed acceptable limits. The recall affects two lots distributed across the United States.
Product
FLUNISOLIDE — FLUNISOLIDE (FLUNISOLIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0012-2023·2022-10-26
Rifampin Capsules recalled due to excess nitrosamine impurity
Golden State Medical Supply Inc. is recalling Rifampin Capsules, 150 mg, due to elevated levels of 1-Methyl-4-Nitrosopiperazine (MNP) exceeding the FDA interim specification limit of 5 ppm. Affected lots are distributed nationwide.
Product
Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V803000·2022-10-25
2022 Porsche 911 GT3 seat belt anchor screws may not be properly tightened
Porsche is recalling certain 2022 911 GT3 vehicles because the screw attaching the lower seat belt anchor may not have been properly tightened. A loose anchor could detach in a crash, increasing injury risk.
Product
PORSCHE — PORSCHE 911 GT3
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23022·2022-10-25
Pine-Sol Multi-Surface and All-Purpose Cleaners Recalled for Bacterial Contamination
Clorox is recalling Pine-Sol cleaners contaminated with Pseudomonas aeruginosa, a bacteria that risks serious infection in immunocompromised people or those with external medical devices. No illnesses have been reported to date.
Product
Pine-Sol® Scented Multi-Surface Cleaners in Lavender Clean®, Sparkling Wave®, and Lemon Fresh scents, CloroxPro® Pine-Sol® All Purpose Cleaners, in Lavender Clean®, Sparkling Wave®, Lemon Fresh, and Orange Energy® scents, and Clorox® Professional™ Pine-Sol® Lemon Fresh Cleaners.…
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·22V801000·2022-10-24
Gillig Recalls 2022 Low Floor Transit Buses Due to Steering Defect
Gillig is recalling 388 2022 Low Floor transit buses because a steering shaft grease fitting may damage a protective shroud, potentially causing loss of steering control.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V800000·2022-10-24
Kia Recalls 2008-2009 Sportage Vehicles for Engine Fire Risk
Kia is recalling 2008-2009 Sportage vehicles because an engine compartment fire may occur from the Hydraulic Electronic Control Unit, increasing injury risk.
Product
KIA — KIA SPORTAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V799000·2022-10-22
CAN-AM Ryker Motorcycles Recalled for Loose Harnesses Causing Engine Stall
CAN-AM is recalling 2019-2023 Ryker motorcycles because electrical harnesses in the front fenders may loosen and rub on the tire, causing a short circuit that can stall the engine while driving.
Product
CAN-AM — CAN-AM RYKER
Category
Vehicle
Distribution
Distributed nationwide