State

District of Columbia product recalls

72,992 recalls have nationwide distribution and so reach DC. 2,795 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total: 2,795
Critical: 240
Severe: 946
Most recent: 2026-09-02

Of the 2,795 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 946 (34%) are Severe.

Which agencies issued them

These figures cover only the 2,795 recalls whose distribution notice names District of Columbia specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8226–8250 of 75787

HighFDA (Devices)·Z-0916-2025·2025-01-22
Cardinal Health Presource Surgical Kits Recalled for Potential Endotoxin Contamination
Cardinal Health is recalling Presource surgical kits due to potential endotoxin contamination in non-sterile surgical strips and patties. The recall affects 512,786 units distributed worldwide.
Product
Cardinal Health Presource Kits: 1) ORTHO PLASTIC MICROVASCULAR PK , Catalog Number: PGVMFFBLY; 2) ORTHO PLASTIC MICROVASCULAR PK , Catalog Number: PGVMFFBLZ; 3) KIT,NEURO SPINE,ANDERSON , Catalog Number: PN23SPAM5; 4) KIT, MAJOR SPINE , Catalog Number: PN33MSOC3; 5) KIT, MAJOR
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0851-2025·2025-01-22
Intuitive Surgical Micro Forceps Recalled Due to Grip Cable Defects
Intuitive Surgical is recalling 8MM Black Diamond Micro Forceps (Model 470033) due to complaints of frayed or broken grip cables. The defect affects 1,111 units distributed nationwide and internationally.
Product
8MM,BLACK DIAMOND MICRO FORCEPS,IS4000 ¿ REF 470033
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0926-2025·2025-01-22
ECONO STERILE Medical Procedure Kits Recalled for Packaging Defects
Sklar Instruments is recalling ECONO STERILE medical procedure kits due to packaging issues that may compromise the sterile barrier and allow contamination.
Product
ECONO STERILE brand medical procedure kits labeled as: 1) ECONO STERILE FREER ELEV DE S/B 7.25" CS/25, Model Number 96-2483 (multiple purpose); 2) ECONO STERILE LOCKE ELEV #94 NARROW STER 25, Model Number 96-2484 (foot procedures)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0901-2025·2025-01-22
Digoxin Test Slides May Report Inaccurately Due to Hemoglobin Interference
QUIDEL ORTHO is recalling VITROS DGXN test slides because hemoglobin can interfere with digoxin measurements at lower-than-expected levels, potentially causing inaccurate test results.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products DGXN Slides Model/Catalog Number: 8343386 Software Version: Not Applicable Product Description: The VITROS DGXN Slide is a multilayered, analytical element coated on a polyester support. Digoxi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0962-2025·2025-01-22
Olympus LithoCrushV Mechanical Lithotriptor Recalled for Distal Tip Tearing Risk
Olympus Corporation recalls the LithoCrushV Single Use Mechanical Lithotriptor due to potential distal tip tearing during endoscopic procedures. The FDA Class II recall affects 989 units distributed nationwide.
Product
LithoCrushV Single Use Mechanical Lithotriptor V. Model Number: BML-V442QR-30. Single Use Mechanical Lithotriptor V used with Olympus endoscope for crushing calculi inside the bile duct.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0908-2025·2025-01-22
Cardinal Health Presource Surgical Kits Recalled for Endotoxin Contamination
Cardinal Health is recalling Presource surgical kits due to potential endotoxin contamination in non-sterile surgical strips and patties. No illnesses have been reported.
Product
Cardinal Health Presource Kits: 1) KIT,PLASTIC FLAP,Catalog Number PGHDOT951; 2) KIT,ORP PLASTIC FLAP,Catalog Number PGHDOT952; 3) KIT,ORP PLASTIC FLAP,Catalog Number PWHDOT910; 4) KIT,ORP PLASTIC FLAP,Catalog Number PWHDOT911; 5) KIT,ORP PLASTIC FLAP,Catalog Number PWHD
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0937-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Surgical Scalpel Handles for Sterile Barrier Risk
Sklar Instruments recalls ECONO STERILE SCALPEL HDL #3 surgical handles due to packaging issues that may compromise the sterile barrier. The 150-unit recall affects units distributed nationwide with lot code SK-125.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCALPEL HDL #3 W/METRIC CS/25, Model Number 96-3500M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0864-2025·2025-01-22
8MM Large Suturecut Needle Driver Recalled for Frayed Grip Cables
Intuitive Surgical is recalling 8MM Large Suturecut Needle Driver instruments due to frayed or broken grip cables. The recall affects 784 units distributed nationwide and internationally.
Product
8MM,LARGE SUTURECUT NEEDLE DRIVER,IS4000¿ REF 470296
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0944-2025·2025-01-22
Gynecological Speculum Kits Recalled for Potential Sterile Barrier Breach
Sklar Instruments is recalling ECONO STERILE gynecological speculum kits due to packaging issues that may compromise sterility. No injuries have been reported.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE GRAVES SPEC STRL SM BX/25, Model Number 96-2603; 2) ECONO STERILE GRAVES SPEC STRL MD BX/25, Model Number 96-2605; 3) ECONO STERILE GRAVES SPEC STRL LG BX/25, Model Number 96-2607; 4) ECONO STERILE PEDER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2025·2025-01-22
Intuitive Surgical Fenestrated Grasper Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling its 8MM Tip-Up Fenestrated Grasper due to frayed or broken grip cables on reusable surgical instruments. The defect affects multiple batch numbers produced between 2023 and 2024.
Product
8MM,TIP-UP FENESTRATED GRASPER,IS4000¿ REF 470347
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0870-2025·2025-01-22
Intuitive Surgical Clip Applier Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling 5,576 units of the 8MM Horizon Small Clip Applier due to complaints of frayed or broken grip cables on the reusable instruments.
Product
8MM,HORIZON SMALL CLIP APPLIER,IS4000¿ REF 470401
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0949-2025·2025-01-22
Sklar Instruments ECONO STERILE surgical procedure kits recalled due to packaging defect
Sklar Instruments is recalling ECONO STERILE ALFONSO INFANT SPEC STRL sterile surgical procedure kits nationwide due to packaging issues that may breach the sterile barrier.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE ALFONSO INFANT SPEC STRL CS/10, Model Number 96-3814; eyelid surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0952-2025·2025-01-22
Orthopedic Surgery Kits Recalled for Potential Sterile Barrier Packaging Defects
Sklar Instruments is recalling ECONO STERILE LEMPERT BONE RONG orthopedic surgery kits due to packaging defects that may compromise sterility. The affected kits (Model 96-4780A, Lot HSI) were distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE LEMPERT BONE RONG 6.25" STER25, Model Number 96-4780A; orthopedic surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0847-2025·2025-01-22
Intuitive Surgical Monopolar Curved Scissors Recalled for Frayed Grip Cables
Intuitive Surgical recalls 355,547 monopolar curved scissors due to increased complaints of frayed or broken grip cables on these reusable surgical instruments.
Product
8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0931-2025·2025-01-22
Medical Procedure Kits Recalled for Potential Sterile Barrier Breach
Sklar Instruments is recalling ECONO STERILE Curette Excavator surgical kits due to packaging issues that may compromise sterile barriers. Affected kits were distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE" CURETTE EXCAVATOR STRL CS/25, Model Number 941-1320; general surgical
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0927-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Trousseau Dilator Kits for Packaging Defects
Sklar Instruments is recalling ECONO STERILE trousseau dilator kits (Model 941-0191) distributed nationwide due to packaging issues that may compromise the sterile barrier. Affected healthcare providers should stop use immediately.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE TROUSSEAU DILATOR CS/25, Model Number 941-0191 (tracheal procedures)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V027000·2025-01-22
Starcraft Bus Recalls 2023-2024 Models for Emergency Exit Handle Issues
Forest River is recalling 2023-2024 Starcraft Starlite and Allstar buses because emergency exit handles are not easily accessible, potentially delaying passenger evacuation.
Product
STARCRAFT BUS — STARCRAFT BUS ALLSTAR, STARLITE
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0919-2025·2025-01-22
OsteoCove and Cove Putty bone void fillers recalled due to hydration defect
IsoTis OrthoBiologics is recalling OsteoCove Putty and Cove Putty bone graft materials due to a hydration issue that makes the product less cohesive and moldable than intended.
Product
OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0195-2025·2025-01-22
Acetaminophen 325 mg tablets recalled for incorrect imprinting
Akron Pharma is recalling 14,825 bottles of Acetaminophen 325 mg tablets due to incorrect tablet imprinting affecting lots KDT0124004, KDT0124005, and KDT0124006 (expiring August 31, 2026). No illnesses have been reported.
Product
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0193-2025·2025-01-22
Acetaminophen Extra Strength tablets recalled for incorrect product imprint identification
Akron Pharma recalls 768 bottles of Acetaminophen Extra Strength 500 mg due to incorrect identification imprinted on the tablets nationwide.
Product
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0204-2025·2025-01-22
Prescription Drug Cardura XL Recalled for Out-of-Specification Impurity
Viatris is recalling Cardura XL (doxazosin) 4 mg extended-release tablets nationwide due to out-of-specification impurity results detected during stability testing.
Product
CARDURA — CARDURA (DOXAZOSIN MESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0196-2025·2025-01-22
Acetaminophen Extra Strength tablets recalled for incorrect imprinting
Akron Pharma is recalling 1,232 bottles of Acetaminophen Extra Strength tablets due to incorrect imprinting on the tablets. The product identification may be wrong on the affected tablets.
Product
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0955-2025·2025-01-22
Demineralized Bone Matrix Putty Recalled for Incorrect Outer Box Expiration Date
IsoTis OrthoBiologics recalls OsteoSurge 100 Demineralized Bone Matrix Putty due to incorrect expiration dates on outer packaging. The outer box date does not match the correct date on the inner tray.
Product
OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix, OsteoSurge 100 Demineralized Bone Matrix, 10cc, REF 56300100.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0401-2025·2025-01-22
Eclectic Herb Vitamin Blend Dietary Supplement Recalled for Label Errors
Eclectic Herb Vitamin Herb Blend dietary supplement is recalled because the Supplement Facts panel contains incorrect ingredient names and quantities. Consumers should check affected lot numbers.
Product
Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham, OR 97030. The affected label declared "Oregon Grape 190mg ***Oregon Grape 97mg***Cayenne Root (Allium
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0942-2025·2025-01-22
Sklar Instruments ECONO STERILE Blackhead Extractor Kits Recall
Sklar Instruments is recalling ECONO STERILE blackhead extractor kits (Model 96-2395M) due to packaging issues that may compromise the sterile barrier. The kits were distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCHAMBERG EXTRCT SQ STER CS25, Model Number 96-2395M; blackhead extractor
Category
Medical Device
Distribution
Distributed nationwide