State

Virginia product recalls

73,198 recalls have nationwide distribution and so reach Virginia. 9,492 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total: 9,492
Critical: 1,286
Severe: 2,302
Most recent: 2026-09-25

Of the 9,492 recalls naming Virginia we have scored against our rubric, 1,286 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,302 (24%) are Severe.

Which agencies issued them

These figures cover only the 9,492 recalls whose distribution notice names Virginia specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12426–12450 of 82690

SevereFDA (Drugs)·D-0486-2024·2024-05-15
Sapropterin Dihydrochloride Powder for Oral Solution Recalled Due to Sub-Potency
Dr. Reddy's Laboratories is recalling 2,402 cartons of Sapropterin Dihydrochloride Powder 100mg due to sub-potency associated with powder discoloration. The affected lot (T2200352) was distributed nationwide.
Product
Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-477-30.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V340000·2024-05-15
2025 MINI Countryman Rear Armrest May Detach During Airbag Deployment
BMW is recalling 9 2025 MINI Countryman vehicles because the armrest support bracket on the rear side door panel may be improperly secured and detach during an airbag deployment, potentially striking occupants or interfering with airbag function.
Product
MINI — MINI COUNTRYMAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0489-2024·2024-05-15
TraMADol HCl 50 mg Tablets Recalled for Foreign Baclofen Tablets
RemedyRepack Inc. is recalling TraMADol HCl 50 mg tablets nationwide after a pharmacist discovered a baclofen tablet in a tramadol bottle. Taking the wrong medication poses serious health risks.
Product
TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: Advagen Pharma Limited, Plainsboro. NJ 08536, Repackaged by: RemedyRepack Inc.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2024·2024-05-15
DURAMAX vascular catheter recalled for possible metal shaving hazard
The DURAMAX STACKED TIP vascular catheter may contain loosely affixed metal shavings that could embolize and require surgical removal. Lot 5807208 affected, 15 units.
Product
DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028191
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-1219-2024·2024-05-15
FDA Recalls Sacramento Cookie Factory Wine Wafers for Undeclared Milk Allergen
Sacramento Cookie Factory recalls Original Wine Wafer - Lemon Vanilla cookies in multiple states due to undeclared milk allergen. Consumers with milk allergies should not consume this product.
Product
Original Wine Wafer - Lemon Vanilla [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Category
Food
Distribution
14 states
HighFDA (Drugs)·D-0493-2024·2024-05-15
Prescription antifungal injection product recalled for out-of-specification assay
Sun Pharmaceutical is recalling Amphotericin B for Injection (50 mg vials) due to out-of-specification assay results. The recall affects 11,016 vials with lot numbers BAE0055A, BAE0056A, and BAE0068A distributed nationwide.
Product
AMPHOTERICIN B — AMPHOTERICIN B (AMPHOTERICIN B)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1220-2024·2024-05-15
Martinelli's Gold Medal Apple Juice Recalled for Elevated Inorganic Arsenic
S Martinelli & Company is recalling Martinelli's Gold Medal Apple Juice (1 Liter) due to elevated levels of inorganic arsenic. The affected product has Best By dates of March 9, 2026 or March 10, 2026.
Product
Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples 1 Liter (33.8 fl oz.) No Additives of Any Kind UPC 0 00 41244 00102 6
Category
Food
Distribution
35 states
HighFDA (Devices)·Z-1767-2024·2024-05-15
FDA Recalls Vascular Access Device Due to Loose Metal Shavings Risk
Angiodynamics' DURAMAX STACKED TIP vascular access device may contain loosely affixed metal shavings that could cause blood vessel blockage, potentially requiring surgical removal.
Product
DURAMAX STACKED TIP 24CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028035
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1781-2024·2024-05-15
GE Allia IGS Fluoroscopic X-Ray Systems Adhesive Bolt Defect
GE Healthcare recalled certain Allia IGS and related fluoroscopic x-ray systems due to potential incomplete adhesive on bolts in the gantry assembly, risking detector or tube failure.
Product
GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1769-2024·2024-05-15
Angiodynamics Duramax Vascular Access Kit Recall Due to Metal Shavings
Angiodynamics recalls the Duramax Stacked Tip vascular access kit used for hemodialysis due to potential loose metal shavings that could enter the bloodstream and require surgical removal.
Product
DURAMAX STACKED TIP 28CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028045
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1783-2024·2024-05-15
GE Healthcare Allia IGS Fluoroscopic Systems Recall: Missing Adhesive
GE Healthcare recalls Allia IGS and related interventional fluoroscopic x-ray systems due to potentially missing adhesive on bolts. The defect could allow the detector/elevator or x-ray tube in the gantry assembly to fall.
Product
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1757-2024·2024-05-15
Philips 5000 Compact Series Ultrasound Systems pose uncontrolled burn risk
Philips 5000 Compact Series ultrasound systems may leave unselected transesophageal transducers powered without temperature monitoring, risking patient burns during imaging procedures.
Product
5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5500 G/795145, and Product/REF: 5300 W/795146, 5300 P/795147, 5300 G/795148, used with Deluxe and Premium Carts that come with multiport adapters.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1760-2024·2024-05-15
Hemodialysis vascular access kit recalled for loose metal shavings
Angiodynamics recalls 455 DURAFLOW 2 hemodialysis kits for loose metal shavings that could embolize, potentially requiring surgical removal.
Product
DURAFLOW 2, 24CM STRAIGHT BASIC KIT -Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012015
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1761-2024·2024-05-15
Vascular access device recalled due to loose metal shavings
DURAFLOW 2 vascular access kits for hemodialysis are being recalled because some units may contain loosely affixed metal shavings that could travel through blood vessels and potentially require surgical removal.
Product
DURAFLOW 2, 28CM STRAIGHT BASIC KIT, 1 per Bx PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012021
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1763-2024·2024-05-15
Duraflow 2 vascular catheter kit recalled for loose metal shavings
Angiodynamics Inc. is recalling DURAFLOW 2 vascular catheter kits used for hemodialysis and apheresis access due to potential metal shavings that may detach and travel through the vascular system, potentially requiring surgical removal.
Product
DURAFLOW 2, 55CM STRAIGHT BASIC KIT PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012115
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1765-2024·2024-05-15
Vascular Access Catheter Recall Due to Metal Shaving Risk
Angiodynamics is recalling 65 DURAFLOW 2 vascular access devices distributed in Virginia due to potential loose metal shavings that could enter the bloodstream and require surgical removal.
Product
DURAFLOW 2, 28CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012195
Category
Medical Device
Distribution
1 state
HighNHTSA·24V344000·2024-05-15
2021-2023 Volkswagen ID.4 display software defect increases crash risk
Certain 2021-2023 Volkswagen ID.4 vehicles experience a software issue causing display failures that hide the speedometer and rearview camera. Dealers will update the software at no cost.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1773-2024·2024-05-15
Vascular catheter recalled for potential metal shavings that may cause embolization
Angiodynamics recalled a vascular access catheter used for hemodialysis because it may contain loosely affixed metal shavings. These shavings could potentially detach and move through blood vessels, possibly requiring surgical removal.
Product
DURAMAX STACKED TIP 32 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028201
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1772-2024·2024-05-15
Angiodynamics vascular access catheter subject to voluntary recall
Angiodynamics has voluntarily recalled 285 units of DURAMAX STACKED TIP vascular access catheters (lots 5807195 and 5807196) used for hemodialysis. The specific reason for the recall is not disclosed in the FDA notice.
Product
DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 5-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028195
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1778-2024·2024-05-15
GE Innova IGS Fluoroscopic X-Ray Systems Adhesive Defect Recall
GE Healthcare is recalling certain Innova IGS x-ray systems due to potential adhesive defects on component bolts. Missing adhesive could cause the detector or x-ray tube to fall during use.
Product
GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2024·2024-05-15
Hemodialysis vascular access kit recalled due to metal shavings risk
DURAMAX hemodialysis vascular access kits are recalled due to potential metal shavings that could enter the bloodstream and require surgical removal. Thirty units distributed in Virginia are affected.
Product
DURAMAX STACKED TIP 28CM STR. BASIC KIT, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028041
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1779-2024·2024-05-15
Interact Discovery RT X-ray Systems Recalled for Component Fall Risk
GE Healthcare is recalling certain x-ray systems because adhesive material may not be properly attached to bolts, which could cause components to fall during use.
Product
GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2024·2024-05-15
Medical Device Recall: Angiodynamics DURAMAX Tunneler with Metal Shavings
Angiodynamics is recalling DURAMAX STACKED TIP medical devices that may contain loosely affixed metal shavings with potential to embolize, requiring possible surgical removal. The recall affects 50 units distributed in Virginia.
Product
DURAMAX STACKED TIP 24CM STR. BASIC KIT, 1-UP PG Product Number: H787103028031
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1784-2024·2024-05-15
X-ray C-arm Tabletop Recalled for Risk of Uncontrolled Motion
NRT X-RAY A/S recalls Intelli-C X-ray tabletops due to faulty firmware and worn motor components that may cause uncontrolled C-arm motion, potentially striking patients or operators.
Product
Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0487-2024·2024-05-15
Tramadol Hydrochloride Tablets Recalled Due to Baclofen Contamination
Advagen Pharma is recalling Tramadol Hydrochloride Tablets after a pharmacy discovered baclofen tablets mixed in a bottle of tramadol. This nationwide recall affects 2,592 bottles.
Product
TRAMADOL HYDROCHLORIDE — TRAMADOL HYDROCHLORIDE (TRAMADOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide