The Recall Desk

State

Virginia product recalls

72,940 recalls have nationwide distribution and so reach Virginia. 9,479 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total
9,479
Critical
1,285
Severe
2,294
Most recent
2026-09-09

Of the 9,479 recalls naming Virginia we have scored against our rubric, 1,285 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,294 (24%) are Severe.

These figures cover only the 9,479 recalls whose distribution notice names Virginia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4101–4125 of 82419

  • CriticalFDA (Devices)·Z-0910-2026·2025-12-17

    Frozen whole surti papdi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen surti papdi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0321-2026·2025-12-17

    Frozen hot green chillies recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen hot green chillies after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Sticker label (for Loose Bulk - yellow peaches): 4044
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0315-2026·2025-12-17

    Peppermint peaches in four pound packs recalled over potential Listeria contamination

    Moonlight Packing is recalling 13,069 cases of 4 lb Peppermint Peach white peaches over potential contamination with Listeria monocytogenes.

    Product
    UPC 8 10248 03087 1 Peppermint Peach WHITE PEACHES READY TO EAT FROM CALIFORNIA PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 8 10248 03163 2 Peppermint Peaches WHITE PEACHES READY TO EAT FROM CALIFORNIA PRODUCE OF U.S.A. NET WT. 4 LBS. M
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·H-0318-2026·2025-12-17

    Peppermint peaches recalled over potential Listeria monocytogenes contamination

    Moonlight Packing is recalling 570 cases of 2 lb Peppermint Peach bags over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.

    Product
    UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS. (907G) MOONLIGHT PACKING CORPORATION REEDLEY, CA 93654
    Category
    Food
    Distribution
    39 states
  • SevereNHTSA·25V873000·2025-12-17

    Suzuki Recalls 2025-2026 DR-Z400 Motorcycles for Brake Fluid Leak Risk

    Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.

    Product
    SUZUKI — SUZUKI DR-Z400SM, DR-Z400S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V876000·2025-12-17

    Wheelchair restraint retractors in converted vans may fail to lock

    Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.

    Product
    HONDA — HONDA, TOYOTA, FORD ODYSSEY, SIENNA, TRANSIT, EXPRESS 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V875000·2025-12-17

    Autocar Recalls 2024 E-ACTT Tractor for Battery Cable Fire Risk

    Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V871000·2025-12-17

    BMW Recalls 2014-2015 Models Due to Head Air Bag Inflator Defect

    BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.

    Product
    BMW — BMW M235I, 228I, 328I, 320I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V872000·2025-12-17

    Toyota Highlander third row seat belt anchor may be installed incorrectly

    Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V877000·2025-12-17

    Chrysler Pacifica wheelchair restraints may not lock securely

    Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.

    Product
    HONDA — HONDA, CHRYSLER, TOYOTA ODYSSEY, PACIFICA, SIENNA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0226-2026·2025-12-17

    Cinacalcet 90 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 12,576 bottles of Cinacalcet Hydrochloride Tablets, 90 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0887-2026·2025-12-17

    Drainage catheter trays recalled over safety indicators showing the wrong position

    Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.

    Product
    Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V874000·2025-12-17

    Kia Sportage instrument panel screen may fail due to software error

    Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.

    Product
    KIA — KIA SPORTAGE, SPORTAGE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0224-2026·2025-12-17

    Cinacalcet 30 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0245-2026·2025-12-17

    Frozen potato gems recalled over semi-rigid plastic fragments embedded inside

    JR Simplot is recalling 7,053 cases of Simplot Traditional Reduced Sodium Tater Gems after pieces of semi-rigid plastic were found embedded in the product.

    Product
    Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master case UPC 100 71179 00418 9. Distributed by Simplot Global Food, LLC, P.O. Box 9386, Boise, ID 83707
    Category
    Food
    Distribution
    19 states
  • ModerateFDA (Drugs)·D-0223-2026·2025-12-17

    Morphine sulfate oral solution recalled over a carton size mismatch

    Winder Laboratories is recalling 3,528 bottles of Morphine Sulfate Oral Solution because the size stated on the carton label did not match the size of the bottle inside.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0908-2026·2025-12-17

    Ureteral stent kits, 8 French, recalled over a size labeling discrepancy

    C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.

    Product
    BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0221-2026·2025-12-17

    Compounded ophthalmic syringes recalled over an incorrect product formulation

    Fagron Compounding Services is recalling 2,980 syringes of a compounded topical ophthalmic solution over an incorrect product formulation.

    Product
    Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution, 0.5mL Single-Use Syringe, For Topical Ophthalmic Use Only. Not for IV Use. Fagron Sterile Services, 8710 E 34th St N, Wichita, KS 67226. NDC: 71266-8240-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0907-2026·2025-12-17

    Ureteral stent kits recalled because the stent size may not match the label

    C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 6 Fr x 30 cm, because the actual stent size may not match the product label.

    Product
    BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0894-2026·2025-12-17

    Sacroiliac fusion screws recalled over labeling claims not consistently present

    Orthofix U.S. is recalling 19,431 FIREBIRD SI Fusion System units because the labeling contains claims that are not consistently present.

    Product
    Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-1030SP 11mm X 30mm FIREBIRD SI Screw; 18-1035SP 11mm X 35mm FIREBIRD SI Screw; 18-1040SP 11mm X 40mm FIREBIRD SI Screw; 18-1045S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0909-2026·2025-12-17

    AMSCO 7052HP washer disinfectors recalled over a wire that may shift

    Steris is recalling 10 AMSCO 7052HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.

    Product
    AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps a
    Category
    Medical Device
    Distribution
    Distributed nationwide