The Recall Desk

State

Maryland product recalls

73,570 recalls have nationwide distribution and so reach Maryland. 8,225 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total
8,225
Critical
996
Severe
2,516
Most recent
2026-10-21

Of the 8,225 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.

Which agencies issued them

These figures cover only the 8,225 recalls whose distribution notice names Maryland specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25801–25825 of 81795

  • ModerateFDA (Drugs)·D-0020-2022·2021-10-27

    GlipiZIDE Extended-Release Tablets 2.5 mg Nationwide Recall

    American Health Packaging is recalling GlipiZIDE Extended-Release Tablets 2.5 mg (Lot #194141) nationwide because dissolution test results exceeded specification, which may affect the drug's effectiveness.

    Product
    GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E090000·2021-10-26

    WABCO Trailer ABS Systems Recalled for Brake Pressure Loss Risk

    WABCO is recalling certain Trailer ABS Systems because improperly tightened screws may loosen, causing pressure loss and potential brake failure.

    Product
    SERVICE BRAKES, AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V837000·2021-10-25

    2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk

    Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V835000·2021-10-25

    Tesla Model 3 and Model Y suspension fasteners recalled for loosening

    Tesla is recalling 2019-2021 Model 3 and 2020-2021 Model Y vehicles where front suspension lateral link fasteners may loosen, potentially causing wheel misalignment and increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V834000·2021-10-25

    2020-2023 Tesla Model 3 Curtain Airbag Deployment Safety Defect

    Tesla is recalling certain 2020-2023 Model 3 vehicles because the side curtain airbag may be improperly secured to the roof rail and could twist, deploying incorrectly during a crash and increasing risk of injury or ejection.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V836000·2021-10-25

    Yamaha Recalls 2021 Tracer 9 GT for Incorrect VIN Label

    Yamaha is recalling 2021 Tracer 9 GT motorcycles because the VIN on the certification label may not match the vehicle's stamped VIN, potentially preventing owners from receiving safety recall remedies.

    Product
    YAMAHA — YAMAHA TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V833000·2021-10-23

    Ferrari Recalls 458 and 488 Models for Brake Fluid Leak Risk

    Ferrari is recalling specific 458 and 488 models because the brake system may leak fluid, potentially causing a loss of braking ability.

    Product
    FERRARI — FERRARI 488 GTB, 458 ITALIA, 488 SPIDER, 458 SPECIALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22007·2021-10-22

    Walmart Better Homes and Gardens Room Spray Recalled for Dangerous Bacteria

    Walmart is recalling Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones due to contamination with Burkholderia pseudomallei bacteria. CDC testing identified the hazard and is investigating a cluster of four melioidosis cases, including two deaths.

    Product
    Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V830000·2021-10-22

    2021-2022 Forest River XLR Toy Hauler Recalled for Missing Furnace Protective Panel

    Forest River is recalling certain 2021-2022 XLR Toy Hauler recreational vehicles with a missing protective panel between the furnace and cargo area. The missing panel could allow cargo to contact furnace wiring, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V828000·2021-10-22

    2022 Coachmen Catalina Travel Trailer Recall for Unsealed Furnace Panel

    Forest River is recalling 2022 Coachmen Catalina travel trailers because an unsealed panel between the furnace and cooktop could cause an inverted flame, increasing fire risk.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V829000·2021-10-22

    2022 Forest River XLR Toy Hauler Recalled for Electrical Fire Risk

    2022 Forest River XLR Toy Hauler RVs are recalled due to incorrect wiring lacking required over-current protection. The defect can cause electrical shorts and fire; dealers will replace the wiring and breaker at no cost.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V832000·2021-10-22

    Mercedes-Benz Recalls 2021 Models for Rear Window Bonding Defect

    Mercedes-Benz is recalling certain 2021 GLE and GLS models because the rear window may be insufficiently bonded, posing a road hazard risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS450, AMG GLE53, GLS580, GLE 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V831000·2021-10-22

    2022 BMW X4 Rear License Plate Lamp Illumination Defect

    BMW is recalling certain 2022 X4 vehicles because the rear license plate may not be properly illuminated, violating federal safety standards and potentially creating visibility issues for other drivers.

    Product
    BMW — BMW X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V827000·2021-10-21

    Orange EV Recalls T-Series Trucks Due to Steering Bolt Issue

    Orange EV is recalling 2019-2021 T-Series electric trucks because a steering bolt may loosen, potentially causing loss of steering.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22702·2021-10-21

    Husqvarna and GASGAS Off-Road Motorcycles Recalled for Front Brake Failure

    About 1,840 Husqvarna and GASGAS off-road competition motorcycles sold from May through August 2021 are being recalled because retaining clips on the front brake caliper can fall out, causing brake failure and crash hazard. No injuries have been reported.

    Product
    Husqvarna and GASGAS Off-Road closed course competition motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22703·2021-10-21

    Lightform LED Projectors Recalled Due to Fire Hazard

    Lightform Inc. is recalling about 1,600 LF2 and LF2+ LED projectors because the fan can malfunction and overheat, posing a fire hazard. No injuries or property damage have been reported.

    Product
    Lightform projectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0005-2022·2021-10-20

    Abbott Alinity m Resp-4-Plex Respiratory Diagnostic Kit Recalled for False Positive Results

    Abbott is recalling the Alinity m Resp-4-Plex AMP Kit, an in vitro diagnostic used for respiratory pathogen testing, due to potential for false positive results affecting approximately 8,469 units distributed worldwide.

    Product
    Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization, US Assay) and Alinity m Resp-4-Plex Application Specification File. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0004-2022·2021-10-20

    Abbott SARS-CoV-2 Diagnostic Kit Recalled for Risk of False Positive Results

    Abbott Molecular is recalling 60,563 units of the Alinity m SARS-CoV-2 Amp Kit due to potential false positive test results. The affected kits were distributed worldwide from September 2021 through January 2023.

    Product
    Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization, US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0089-2022·2021-10-20

    FDA recalls Eco-Med ultrasound gels due to bacterial contamination risk

    FDA recalls ultrasound gels manufactured by Eco-Med Pharmaceutical due to possible bacterial contamination. Healthcare providers and facilities should stop use immediately.

    Product
    EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel, Model No. 250UG-CMU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0009-2022·2021-10-20

    Glucagon Emergency Kit Recall: Subpotent Drug in Vials

    Eli Lilly is recalling Glucagon Emergency Kits (Lot #D239382D, expiration April 2022) because some vials contain liquid instead of powder and do not deliver the full expected drug effect when administered.

    Product
    Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285; Glucagon, NDC: 0002-8031-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0018-2022·2021-10-20

    Tone's Taco Seasoning Blend recalled due to undeclared wheat

    B&G Foods North America, Inc. is recalling Tone's Taco Seasoning Blend in plastic bottles because the product contains undeclared wheat, which poses a risk to consumers with wheat allergies.

    Product
    Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, due to the
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Devices)·Z-0006-2022·2021-10-20

    Abbott Alinity m SARS-CoV-2 Amp Kit Recalled for Potential False Positive Results

    Abbott Molecular has recalled 71,314 units of the Alinity m SARS-CoV-2 Amp Kit due to potential false positive results. The kit was distributed worldwide.

    Product
    Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0067-2022·2021-10-20

    FDA Recalls Ultrasound Gels and Lotions for Potential Bacterial Contamination

    Ultrasound gels and lotions from National Distribution & Contracting Inc are being recalled due to potential bacterial contamination. About 25,103 units distributed nationwide and in Canada are affected.

    Product
    ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Ultrasound Transmission Clr 8.5 oz BTL 24/cs ECO 40JMC Gel Ultrasound Transmission Clr 5L 4/cs NDC P301008 ProAdvantage Gel Ultrasound Transmission 8.5 oz 12/cs NDC P301105 ProAdvantage Gel Ultrasound Transmission 5 Liter…
    Category
    Medical Device
    Distribution
    Distributed nationwide