The Recall Desk

State

Maryland product recalls

72,971 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.

These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6476–6500 of 81189

  • SevereFDA (Food)·H-0167-2025·2025-07-09

    ZENSHI Handcrafted Sushi Hawaiian Roll Recalled for Salmonella Risk

    Harris Teeter is recalling ZENSHI Handcrafted Sushi Hawaiian Roll products because the cucumbers used in production were recalled due to possible Salmonella contamination.

    Product
    ZENSHI HANDCRAFTED SUSHI Hawaiian Roll - Salmon, Tuna 10pc (Brown Rice) Net Wt. 10.6oz UPC 0 23012 94365 3
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0504-2025·2025-07-09

    Zicam cold remedy nasal swabs recalled over fungal contamination

    Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.

    Product
    ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0187-2025·2025-07-09

    ZENSHI Handcrafted Sushi Spicy Roll Salmon recalled for Salmonella

    Harris Teeter is recalling ZENSHI Handcrafted Sushi Spicy Roll - Salmon 10pc due to possible Salmonella contamination from recalled cucumbers used in the product.

    Product
    ZENSHI HANDCRAFTED SUSHI Spicy Roll - Salmon 10pc Net Wt. 7.1oz UPC 0 23012 94312 7 & 0 23012 95148 1
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0184-2025·2025-07-09

    Zenshi spicy California roll trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Spicy California Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 30,174 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Spicy California Roll 10pc Net Wt. 7.4oz UPC 0 23012 94404 9 & UPC 0 23012 95146 7
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2015-2025·2025-07-09

    Servo-u MR Ventilator System inaccurate patient circuit compliance measurement

    Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.

    Product
    Servo-u MR Ventilator System. Model Number: 6888800.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0155-2025·2025-07-09

    Zenshi salmon avocado and rainbow duo combo used recalled cucumbers

    Zenshi Handcrafted Sushi Duo Combo with Salmon Avocado and Rainbow Roll is being recalled over cucumbers recalled for possible Salmonella. 6,499 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Duo Combo - Salmon Avocado & Rainbow Roll 10pc Net Wt 7.9oz UPC 0 23012 94207 6
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0163-2025·2025-07-09

    Zenshi happy heart rainbow red rock platters used recalled cucumbers

    Zenshi Handcrafted Sushi Happy Heart Platter #2 is being recalled over cucumbers recalled for possible Salmonella. 2,609 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Happy Heart Platter #2 (Rainbow Red Rock) 13pc Net Wt. 14.9oz UPC 0 23012 94483 4
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0122-2025·2025-07-09

    Zenshi California roll trays made with recalled cucumbers

    Zenshi Handcrafted Sushi California Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 39,743 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI California Roll 10pc Net Wt. 7.1oz (201g) UPC 0 23012 94264 9, UPC 023012 95138 2 & UPC 0 23012 90618 4
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0124-2025·2025-07-09

    Zenshi California salad brown rice rolls made with recalled cucumbers

    Zenshi Handcrafted Sushi California Salad Roll on brown rice is being recalled over cucumbers recalled for possible Salmonella. 240 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI California Salad Roll 10pc (Brown Rice) Net Wt. 7.1oz (201g) UPC 0 23012 94267 & 0 UPC 0 23012 95139 9
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0183-2025·2025-07-09

    Zenshi salmon and cucumber sashimi sampler used recalled cucumbers

    Zenshi Handcrafted Sushi Sashimi Sampler with salmon and cucumber is being recalled over cucumbers recalled for possible Salmonella. 70 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Sashimi Sampler - Salmon w/Cucumber 6pc Net Wt. 4.5oz UPC 0 23012 94305 9
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0197-2025·2025-07-09

    Zenshi ultimate chili tuna roll trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Ultimate Chili Roll with tuna is being recalled over cucumbers recalled for possible Salmonella. 1,365 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Ultimate Chili Roll - Tuna 10pc Net Wt. 10.4oz UPC 0 23012 94413 1
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0200-2025·2025-07-09

    Zenshi yuzu teriyaki sauce trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Yuzu Teriyaki Sauce is being recalled because it was made with cucumbers recalled over possible Salmonella. 39 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Sauce 3oz Net Wt. 3oz UPC 0 23012 95076 7
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0153-2025·2025-07-09

    Zenshi crunchy California and rainbow duo combo used recalled cucumbers

    Zenshi Handcrafted Sushi Duo Combo with Crunchy California and Rainbow Roll is being recalled over cucumbers recalled for possible Salmonella. 5,238 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Duo Combo - Crunchy CA & Rainbow Roll 10pc Net Wt 8.6oz UPC 0 23012 94206 9
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-2044-2025·2025-07-09

    Medline IV Catheter Kits Recalled Over Needle Retraction Issue

    Medline is recalling 36 Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN due to a potential needle retraction failure during insertion.

    Product
    Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2051-2025·2025-07-09

    Philips C9-5EC Ultrasound Transducer Devices Recalled

    Philips Ultrasound, Inc. is recalling Philips C9-5EC transducer devices that were refurbished beyond their useful life, which may affect device performance and safety.

    Product
    Philips C9-5EC Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0501-2025·2025-07-09

    Compounded ketamine multi-dose vials recalled over sterility assurance concerns

    Ketamine Hydrochloride Injection 500 mg/5 mL multi-dose vials compounded by Medivant Healthcare are being recalled for lack of assurance of sterility. 14,725 vials are affected.

    Product
    KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0007-2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2045-2025·2025-07-09

    Medline retinal packs recalled because catheter needle may fail to retract

    Medline RETINAL PACK-LF convenience kits are being recalled because the BD Insyte Autoguard catheter needle inside may be slow to retract or fail to retract during insertion. 80 units affected.

    Product
    Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: RETINAL PACK-LF, REF DYNJ0151148B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2040-2025·2025-07-09

    VITROS 4600 chemistry systems may report results using expired diluent packs

    VITROS 4600 Chemistry Systems are being recalled because a software anomaly can allow results to be reported using diluent packs the system treats as expired, which can produce erroneous results.

    Product
    Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software Version: version 3.2 to version 3.8.3 (all available software versions) Product Description: In vitro diagnostic chemistry analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0502-2025·2025-07-09

    Compounded lidocaine with epinephrine vials lack assurance of sterility

    Lidocaine HCl Sterile Injection 1% with epinephrine 1:100,000, compounded by Medivant Healthcare, is being recalled for lack of assurance of sterility. 2,825 vials affected.

    Product
    LIDOcaine HCL Sterile Injection, USP, 100mg/10mL, 1%, (10mg/mL), w/EPINEPHRINE 1:100,000, For Infiltration & Nerve Block, Including Caudal & Epidural Use, 10 mL Sterile Single-Dose Vial, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2089-2025·2025-07-09

    ADVIA Hematology System Control Product Recall for Platelet Value Error

    Siemens Healthcare Diagnostics is recalling 3,266 units of ADVIA 120/2120/2120i 3-in-1 TESTpoint Control worldwide due to incorrect platelet value assignments that could affect test results.

    Product
    ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0138-2025·2025-07-09

    Harris Teeter Sushi Rolls Recalled Over Salmonella Risk

    Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll trays because the cucumbers used in the sushi may be contaminated with Salmonella.

    Product
    ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll 10pc Net Wt 8.1oz UPC 0 23012 94283 0 & UPC 0 23012 95144 3
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-2072-2025·2025-07-09

    Cardiology hemodynamics software update may cause unexpected system shutdowns

    Change Healthcare Cardiology Hemodynamics Software version 15.0.1 is being recalled because, following complaints, a software update may cause the software to unexpectedly shut down.

    Product
    Change Healthcare Cardiology Hemodynamics Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0498-2025·2025-07-09

    Compounded preservative-free lidocaine vials lack assurance of sterility

    Preservative-free Lidocaine HCl Injection 1%, compounded by Medivant Healthcare, is being recalled for lack of assurance of sterility. 29,700 vials are affected.

    Product
    LIDOcaine HCl Injection, USP, 10mg/mL, 1% (100 mg/10mL), 10 mL Sterile Single Dose Vial, Rx Only, For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative-Free, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S Kyrene Rd., Chandler, AZ, 8522
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2076-2025·2025-07-09

    Bard Urologist's Tray Recalled Over Incorrect French Size Labeling

    C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.

    Product
    REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
    Category
    Medical Device
    Distribution
    Distributed nationwide