The Recall Desk

State

Maryland product recalls

73,388 recalls have nationwide distribution and so reach Maryland. 8,224 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total
8,224
Critical
996
Severe
2,516
Most recent
2026-10-06

Of the 8,224 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,516 (31%) are Severe.

These figures cover only the 8,224 recalls whose distribution notice names Maryland specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20151–20175 of 81612

  • HighNHTSA·22V904000·2022-12-08

    2019-2022 RAM Pickup Trucks Recalled for Defective Tailgate Latch

    Chrysler is recalling 2019-2022 RAM 1500, 2500, and 3500 pickup trucks because the tailgate may not latch properly due to misaligned strikers. An unintended tailgate opening while driving could result in cargo loss and increased crash risk.

    Product
    RAM — RAM 3500, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23057·2022-12-08

    Cordless Window Shades Battery Packs Recalled for Fire Hazard

    About 56,000 lithium-ion battery packs used in cordless window blinds are being recalled because they can overheat and pose a fire hazard. The firm has received reports of overheating and one fire in a commercial warehouse, though no consumer injuries have been reported.

    Product
    Cordless Window Shades Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V909000·2022-12-08

    School buses recalled for incorrectly tightened rear axle fasteners

    Navistar is recalling certain 2023-2024 IC BUS school buses due to fasteners on the rear axle that may have been tightened incorrectly. This can allow the rear axle to shift, reducing vehicle control and increasing crash risk.

    Product
    IC BUS — IC BUS CESB, RESB, EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V903000·2022-12-08

    GM recalls multiple 2020-2023 vehicles for daytime running light control defect

    General Motors is recalling multiple 2020-2023 models because daytime running lights may fail to turn off when headlights are on, creating glare and visibility hazards.

    Product
    BUICK — BUICK, GMC, CADILLAC ENVISION, SIERRA 1500, YUKON, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23063·2022-12-08

    Life is Good Darkest Blue Fleece Sweatshirts and Shorts Recall

    The Life is Good Company is recalling approximately 750 Fall 2022 Darkest Blue fleece sweatshirts and men's shorts that fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.

    Product
    Fall 2022 Darkest Blue Fleece Women's Sweatshirts and Men's Shorts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0354-2023·2022-12-07

    Alcon Surgical Procedure Packs Recalled for Adhesive Defect and Skin Injuries

    Alcon is recalling Custom Pak Surgical Procedure Packs because the adhesive liner is difficult to remove and the manufacturer has observed an increase in skin injuries related to the adhesive.

    Product
    Alcon Custom Pak Surgical Procedure Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0324-2023·2022-12-07

    CoViPoint COVID Test Kits Distributed Without FDA Approval or Clearance

    GS Biomark LLC distributed approximately 639,200 CoViPoint COVID test kits without FDA approval, clearance, or authorization across multiple US states.

    Product
    CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200 BM-D4K0200 BM-DK0200 BM-DK0600 BM-DK0800 BM-DK1200 BM-DK1400 BM-DK1800
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0347-2023·2022-12-07

    Medical laboratory reagent recalled for potential false-negative test results

    Greer Laboratories recalled a hypersensitivity pneumonitis test reagent (Lot 389591) due to decreased reactivity that could cause false-negative results. The issue affects 218 units distributed across 12 U.S. states and two countries.

    Product
    GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0346-2023·2022-12-07

    Diagnostic Kit Recalled for False Positive Bacterial Identification Results

    Accelerate Diagnostics is recalling the Accelerate PhenoTest BC kit due to improperly formulated FISH probes that produce false positive identification results for Staphylococcus aureus and Streptococcus species. Approximately 7,160 kits have been distributed across the United States and internationally.

    Product
    Accelerate PhenoTest BC kit REF 10102018
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0345-2023·2022-12-07

    Accelerate PhenoTest BC Kit Recall Due to False Positive Bacterial Identification

    Accelerate Diagnostics is recalling 200 kits of the Accelerate PhenoTest BC diagnostic test due to improperly formulated FISH probes that may produce false positive results for Staphylococcus aureus and Streptococcus bacteria.

    Product
    Accelerate PhenoTest BC kit REF 10101018
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0340-2023·2022-12-07

    Intuitive Da Vinci Stapler Instruments Recalled for Potential Staple Deployment Failure

    Intuitive Surgical is recalling Da Vinci Xi surgical stapling instruments due to potential staple deployment failure and device fragment generation. No injuries have been reported.

    Product
    INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm Gray 4-Row 2.0 mm Xi|X REF 48230M INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm White 4-Row 2.5 mm Xi|X REF 48230W INTUITIVE Da Vinci 8mm…
    Category
    Medical Device
    Distribution
    24 states
  • HighNHTSA·22V902000·2022-12-07

    Nova Bus Recalls LFS Models for Non-Standard Auxiliary Lighting

    Nova Bus is recalling 2009-2021 LFS and LFS Artic transit buses because non-standard color auxiliary lights may distract other drivers and increase crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0072-2023·2022-12-07

    FDA recalls prescription desmopressin acetate tablets for subpotency

    Heritage Pharmaceuticals' desmopressin acetate tablets (0.2mg) have been recalled nationwide due to subpotency. The voluntary recall affects 13,805 bottles; no illnesses have been reported.

    Product
    DESMOPRESSIN ACETATE — DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0348-2023·2022-12-07

    Medical device test system recalled for decreased reactivity and false-negative results

    Greer Laboratories recalled a hypersensitivity pneumonitis test kit (102 units, Lot 389592) after stability testing revealed decreased reactivity that could cause false-negative results. The issue was discovered in October 2021.

    Product
    GREER DIA - KIT ANTIGEN M. FAENI, 2.0mL 20 MG/ML, Analyte Specific Reagent, Item: K62, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-0180-2023·2022-12-07

    Amy's Kitchen Gluten Free Bean and Cheese Burritos Recalled for Plastic Contamination

    Amy's Kitchen is recalling Gluten Free Bean and Cheese Burritos (Lot 30H0922, best before 08/2024) due to potential plastic pieces in the product. Approximately 5,134 cases were distributed to 18 U.S. states.

    Product
    Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC - 042272-00353-2 Frozen INGREDIENTS: ORGANIC PINTO BEANS, FILTERED WATER, ORGANIC BROWN RICE, ORGANIC GARBANZO BEAN FLOUR, ORGANIC TOMATO PUR¿E, WHITE CHEDDAR…
    Category
    Food
    Distribution
    18 states
  • HighFDA (Drugs)·D-0071-2023·2022-12-07

    Daytrana transdermal methylphenidate patches recalled for adhesive defect

    Noven Pharmaceuticals recalls 3,977 boxes of Daytrana methylphenidate transdermal patches nationwide due to defective adhesive properties in lot 91316. Affected patches may fail to adhere properly or deliver medication inconsistently.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0179-2023·2022-12-07

    Coolhaus Dairy Free Frozen Dessert Recalled for Coliform Detection

    Coolhaus Dairy Free Cookie Dough Lyfe frozen dessert sandwiches recalled due to coliform detected in lab samples. Product distributed to select retailers in Texas, Maryland, Colorado, and California.

    Product
    Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5 Distributed by Coolhaus 8688 Washington Blvd. Culver City, CA 90232
    Category
    Food
    Distribution
    4 states
  • ModerateNHTSA·22V901000·2022-12-07

    Audi Recalls 2023 S3, RS3, and A3 for Missing Weight Label

    Volkswagen Group of America is recalling 2023 Audi S3, RS3, and A3 vehicles because the B-pillar safety label is missing weight capacity information.

    Product
    AUDI — AUDI S3, RS 3, A3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0074-2023·2022-12-07

    Acella Recalls Sodium Sulfacetamide Cleansing Pads for Subpotency

    Acella Pharmaceuticals is recalling Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads because testing found the drug out of specification for potency at shelf-life expiration. 528 cartons distributed nationwide are affected.

    Product
    Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads, Net weight 3.7g (60 cleansing pads Net weight 3.7 g each per carton,) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 300025, NDC 42192-113-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0073-2023·2022-12-07

    Allergy Relief D tablets recalled for failed dissolution specifications

    Dr. Reddy's Laboratories is recalling Allergy Relief D extended-release tablets distributed nationwide by Walmart due to failed dissolution specifications. No illnesses or injuries have been reported.

    Product
    Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V899000·2022-12-06

    Kia Recalls 2020 Niro EV Vehicles for EPCU Coolant Leak Risk

    Kia is recalling 2020 Niro EV vehicles because a coolant leak in the Electric Power Control Unit may cause loss of drive power, increasing crash risk.

    Product
    KIA — KIA NIRO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V898000·2022-12-06

    Hino Recalls 2022-2023 Trucks Due to Fuel Pickup Tube Defect

    Hino is recalling 970 specific 2022-2023 models because a fuel tube may restrict fuel flow, potentially causing engine stalls and increasing crash risk.

    Product
    HINO — HINO NJ7A, NJ7B, NV7A, NE7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V900000·2022-12-06

    KTM 1290 Super Duke R Motorcycles Recalled for Electrical Wiring Defect

    KTM is recalling 2020-2022 1290 Super Duke R motorcycles because the main wiring harness may be misrouted or missing parts, potentially causing an electrical short-circuit and engine stall.

    Product
    KTM — KTM 1290 SUPER DUKE R
    Category
    Vehicle
    Distribution
    Distributed nationwide