The Recall Desk

State

Maryland product recalls

72,984 recalls have nationwide distribution and so reach Maryland. 8,218 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total
8,218
Critical
996
Severe
2,131
Most recent
2026-09-09

Of the 8,218 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 2,131 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7301–7325 of 81202

  • SevereCPSC·25247·2025-05-01

    SharkNinja Foodi Multi-Function Pressure Cookers Recalled for Burn Hazard

    SharkNinja is recalling about 1.8 million Foodi OP300 Series pressure cookers because the pressure-cooking lid can open during use, causing hot contents to escape and burn injuries. The company has received 106 reports of burn injuries, including more than 50 second- or third-degree burns.

    Product
    SharkNinja Foodi OP300 Series Multi-Function Pressure Cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V285000·2025-05-01

    Jayco Recalls 2025 Entegra Launch and Terrain Motorhomes for Electrical Defect

    Jayco is recalling 2025 Entegra Launch and Terrain motorhomes because a standard outlet was installed in the kitchen instead of a GFCI protected outlet, increasing the risk of electric shock.

    Product
    ENTEGRA — ENTEGRA, JAYCO LAUNCH, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25246·2025-05-01

    Kohl's Tea Light Candle Holders Recalled Due to Fire Hazard

    Kohl's is recalling about 1,960 St. Nicholas Square Christmas Tea Light Candle Holders because they can catch on fire, posing a fire and burn hazard. Two fires have been reported with no injuries.

    Product
    St. Nicholas Square Christmas Tea Light Candle Holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25244·2025-05-01

    Santa Cruz Heckler 9 Electric Bicycles Recalled Due to Fire Hazard

    Santa Cruz Bicycles is recalling about 2,850 Heckler 9 electric bicycles due to a fire hazard in the lithium-ion battery. The firm has received three reports of fires with some property damage but no reported injuries.

    Product
    Heckler 9 Electric Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25249·2025-05-01

    Kubota RTV-Series Utility Vehicles Recalled for Crash Hazard

    Kubota is recalling about 49,640 RTV-series utility vehicles because the ball joint on the front suspension can loosen and separate, causing drivers to lose wheel support and risking a crash. No injuries have been reported.

    Product
    Kubota Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25245·2025-05-01

    Dlesot Snap Children's Hair Clips Recalled for Lead Paint Hazard

    Dlesot Snap Hair Clips contain lead paint levels exceeding the federal ban, posing a lead poisoning hazard to children. Approximately 3,800 units were sold on Amazon from April through September 2024.

    Product
    Dlesot Snap Hair Clips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V286000·2025-05-01

    Brinkley RV fifth-wheel trailers recalled for detaching step assembly

    Brinkley RV is recalling 2024-2025 Model G and Model Z fifth-wheel trailers with potentially detaching step assemblies. The clip-on bracket bolts may loosen, causing steps to detach and increasing injury risk.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL G, MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V283000·2025-05-01

    2025 Keystone Kodiak Travel Trailers Recalled for Defective Patio Support Struts

    Keystone is recalling certain 2025 Kodiak travel trailers because the patio support struts may not adequately support the fold-down patio's weight, increasing the risk of injury. Owners should contact Keystone or their dealer for free repair.

    Product
    KEYSTONE — KEYSTONE KODIAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·PHA-05012025-002·2025-05-01

    USDA Issues Public Health Alert for Ineligible Imported Pork Crackling Chips

    USDA FSIS issued a public health alert for mixed potato chip products containing pork cracklings imported from Colombia, a country ineligible to export meat to the U.S.

    Product
    FSIS Issues Public Health Alert for Ineligible Pork Cracklings Products Imported From the Republic of Colombia
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1644-2025·2025-04-30

    Amplatzer TorqVue LP Catheter Recalled for Shaft Breach Risk

    Abbott is recalling the Amplatzer TorqVue LP Catheter (Model 9-TVLPC4F90/080) due to a potential small breach in the proximal shaft that may not be visible and could lead to prolonged procedures, blood loss, or air embolism.

    Product
    Amplatzer TorqVue LP Catheter (TVLPC), Model no. 9-TVLPC4F90/080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0371-2025·2025-04-30

    Dexmedetomidine HCl Syringes Recalled for Potential Sterility Issue

    Leiters Health is recalling dexmedetomidine HCl PF syringes nationwide due to leaking or damaged syringes that may not maintain sterility. Affected lot 2431276A has an expiration date of 4/20/2025.

    Product
    dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0369-2025·2025-04-30

    Haloperidol Decanoate Injection Recalled Due to Sterility Concerns

    Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection vials nationwide because some media fill units showed bacterial contamination, indicating a lack of sterility assurance. The affected product is a 100mg/mL injectable antipsychotic medication.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0367-2025·2025-04-30

    Haloperidol Decanoate Injection Recalled Due to Sterility Concerns

    Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The drug is used for intramuscular injection to treat psychiatric conditions.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0368-2025·2025-04-30

    Haloperidol Decanoate Injection Recalled for Lack of Sterility Assurance

    Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The affected product was distributed nationwide.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1643-2025·2025-04-30

    Amplatzer TorqVue LP Delivery System Recall for Shaft Breach

    Abbott is recalling specific lots of the Amplatzer TorqVue LP Delivery System due to a possible small breach in the shaft that is not visible but could lead to prolonged procedures, blood loss, or air embolism.

    Product
    Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0374-2025·2025-04-30

    Rocuronium Bromide Syringes Recalled Due to Sterility Assurance Risk

    Denver Solutions, LLC DBA Leiters Health is recalling Rocuronium Bromide 50 mg per 5mL syringes due to potential leaking or damage that may compromise sterility assurance.

    Product
    Rocuronium Bromide 50 mg per 5mL (10mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-004-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0372-2025·2025-04-30

    PHENYLephrine HCl Injection Syringes Recalled for Lack of Sterility

    Denver Solutions, LLC DBA Leiters Health is recalling PHENYLephrine HCl 0.5 mg per 5mL single-dose syringes because some syringes may be leaking or damaged, which could compromise sterility assurance.

    Product
    PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0373-2025·2025-04-30

    Ketamine HCl Syringes Recalled for Lack of Sterility Assurance

    Denver Solutions, LLC is recalling Ketamine HCl 50mg per 5mL single-dose syringes nationwide due to leaking or damaged syringes that may lack sterility assurance. Two affected lots are identified with expiration dates in July 2025.

    Product
    Ketamine HCl 50mg per 5mL (10 mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112.NDC: 71449-068-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1656-2025·2025-04-30

    CELL-DYN Ruby hematology analyzer medical device recall

    Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because expired reagents may be used without user notification when scanned or manually entered into the system, contrary to manufacturer guidelines.

    Product
    Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 04U42-84 Software Version: All software versions Product Description: CELL-DYN Ruby
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1654-2025·2025-04-30

    Abbott CELL-DYN Ruby hematology analyzer affected by expired reagent date masking

    Abbott is recalling the CELL-DYN Ruby hematology analyzer because expired reagents may have their expiration dates automatically changed to current or future dates without user notification, potentially leading to use of expired reagents.

    Product
    Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-10 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1655-2025·2025-04-30

    CELL-DYN Ruby hematology analyzer system expiration date validation

    Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers (model 08H67-13) because expired reagents can be used without proper notification when their expiration dates are scanned or entered into the system.

    Product
    Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-13 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1623-2025·2025-04-30

    Medtronic NIM Vital Nerve Monitoring System Software Version Recall

    Medtronic is recalling NIM Vital Nerve Monitoring Systems with software versions v1.6.4 or earlier due to potential increased stimulus artifact that may require troubleshooting and could lead to procedure delay, extubation, and medical intervention.

    Product
    NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED, REF: NIM4CM01RF; PATIENT INTERFACE NIM4CPB1 NIM 4.0, REF: NIM4CPB1; PATIENT INTFC NIM4CPB1RF NIM 4.0 REFURB, REF: NIM4CPB1RF; SOFTWARE NIM4SWU143 UPGRA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1652-2025·2025-04-30

    CELL-DYN Ruby Hematology Analyzer Expiration Date Software Defect

    Abbott's CELL-DYN Ruby hematology analyzer may accept expired reagents without alerting the operator, potentially allowing use of expired materials in patient testing.

    Product
    Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2025·2025-04-30

    Philips Brilliance CT Big Bore X-Ray System Gantry Motion Collision Hazard

    Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.

    Product
    Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1663-2025·2025-04-30

    Skytron Freedom Monitor Mount Hardware Recall for Inadequate Thread Engagement

    The mounting hardware supplied with the Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount does not provide adequate thread engagement to support the weight of the frame and monitor, creating a risk of hardware failure and separation.

    Product
    Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
    Category
    Medical Device
    Distribution
    Distributed nationwide