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.

20726–20750 of 81612

  • SevereFDA (Food)·F-1796-2022·2022-10-05

    Aged Raw Milk Cheese Recalled Due to Listeria Monocytogenes Risk

    Keswick Creamery at Carrock Farms LLC is recalling Vulkwin's Folly Scratch 2 aged raw milk cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.

    Product
    Aged raw milk cheese "Vulkwin's Folly Scratch 2" 4oz-12oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1800-2022·2022-10-05

    Whole Milk Ricotta Cheese Recall Due to Listeria Contamination Risk

    Keswick Creamery is recalling Whole Milk Ricotta cheese sold at farm stores and farmers markets in DC, MD, VA, and PA regions due to potential Listeria monocytogenes contamination.

    Product
    Pasteurized milk cheese "Whole Milk Ricotta" 8 oz and 16 oz clear deli container, expiration dates 7/18/22, 7/25/22, 8/1/22, 8/8/22, 8/18/22
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1810-2022·2022-10-05

    Dutch Red Potatoes with Mustard Sauce Recalled for Undeclared Egg Allergen

    World Variety Produce is recalling Dutch Red Potatoes with Dijon Mustard Sauce because the sauce packet fails to declare the presence of egg, a common allergen. Consumers with egg allergies who consume the product risk allergic reactions.

    Product
    Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World Variety Produce, Inc. Los Angeles, CA Product of USA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1803-2022·2022-10-05

    Pasteurized Quark Cheese Recalled for Potential Listeria Contamination

    Keswick Creamery is recalling Pasteurized Quark cheese due to potential Listeria monocytogenes contamination. The cheese was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.

    Product
    Pasteurized milk cheese "Quark", multiple flavors "Dill and Onion", and "Plain" 8 oz and 16 oz clear deli container, expiration dates 7/7/22, 8/4/22, 8/25/22
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-1763-2022·2022-10-05

    TANDEM LIFE controller software failures affecting cardiopulmonary bypass equipment nationwide

    FDA recalls TANDEM LIFE LivaNova LIFESPARC Controllers due to critical software failures that cause the device to freeze, crash, or stop displaying data. The controllers are used in cardiopulmonary bypass procedures.

    Product
    TANDEM LIFE LivaNova LIFESPARC Controller; Controller and Accessories Model 5900-0000; Controller Only Model 5900-0001. For circulatory or cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1798-2022·2022-10-05

    Aged Raw Milk Cheese Recalled for Listeria Contamination Risk

    Keswick Creamery recalls Calverley aged raw milk cheese due to potential Listeria monocytogenes contamination affecting products distributed to farm stores and farmers markets in DC, MD, VA, and PA.

    Product
    Aged raw milk cheese "Calverley" 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1801-2022·2022-10-05

    Pasteurized Havarti cheese recalled for potential Listeria contamination

    Keswick Creamery is recalling Havarti cheese due to potential Listeria monocytogenes contamination. All products manufactured by the firm may be affected.

    Product
    Pasteurized milk cheese "Havarti" 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1799-2022·2022-10-05

    Aged Raw Milk Feta Cheese Recalled for Listeria Risk

    Keswick Creamery is recalling aged raw milk feta cheese due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in DC, Maryland, Virginia, and Pennsylvania.

    Product
    Aged raw milk cheese "Feta" in 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·22V740000·2022-10-05

    Blue Bird Recalls 2022-2023 Vision Transit Buses Due to Fuel Leak Risk

    Blue Bird is recalling 2022-2023 Vision transit buses with 7.3L gasoline engines because a transmission cable may cause a fuel leak, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1795-2022·2022-10-05

    Aged raw milk cheese recalled for potential Listeria monocytogenes contamination

    Keswick Creamery is recalling Ploughman Cider Wash Tomme aged raw milk cheese (batch 47) due to potential Listeria monocytogenes contamination. The product was distributed to farm stores and farmers markets in Washington DC, MD, VA, and PA.

    Product
    Aged raw milk cheese "Ploughman Cider Wash Tomme" batch 47 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1804-2022·2022-10-05

    Vermeer Cheese Products Recalled for Potential Listeria Contamination

    Keswick Creamery is recalling Vermeer Cheese due to potential Listeria monocytogenes contamination. Products were distributed to farm stores and farmers markets in Washington DC, Maryland, Virginia, and Pennsylvania.

    Product
    Vermeer Cheese in 4 oz to 12 oz packages
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1805-2022·2022-10-05

    Alexia Organic Seasoned Hashed Browns recalled for potential Listeria contamination

    Lamb Weston Sales is recalling Alexia Organic Seasoned Hashed Browns Yukon Select Potatoes due to potential Listeria monocytogenes contamination. The frozen product was distributed nationwide and internationally.

    Product
    Item AX058, Alexia Organic Seasoned Hashed Browns Yukon Select Potatoes, 16 oz. bag, 12/16 oz. bags per case. Product is frozen and it's not ready to eat and labeled with cooking instructions. Produced by Lamb Weston, Kennewick, WA. UPC 8 34183 00303 5. Product contains…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1855-2022·2022-10-05

    Medline ClearPro Suction Catheter Connector May Separate During Use

    Medline ClearPro closed suction catheters may have a connector that separates from the device during patient suctioning. The malfunction affects 65,320 units distributed nationwide and internationally.

    Product
    MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. ET LENGTH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12; b. ET LENGTH DOUBLE SWIVEL, 14 Fr, Item…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1830-2022·2022-10-05

    Cope Mandril Wire Guide Guidewires Recalled for Packaging Seal Breach

    Cook Incorporated is recalling Cope Mandril Wire Guide stainless steel guidewires because the packaging chevron seal may be completely breached, compromising device sterility. Affected lots total 2,748 units in the US and 302 internationally.

    Product
    Cope Mandril Wire Guide (Stainless Steel), Stainless Steel Guidewire Reference Part Number/GPN PMG-18SP-60-COPE G05183 PMG-18SP-100-COPE G05822 PMG-18SP-125-COPE G10077
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1839-2022·2022-10-05

    Cook Roadrunner Guidewire Recalled for Compromised Sterile Packaging Seal

    Cook Incorporated is recalling Roadrunner PC Wire Guide guidewires due to a complete breach of the sterile packaging seal. The breach may compromise device sterility, affecting 202 units in the US and 11 internationally.

    Product
    Roadrunner PC Wire Guide (Nimble Floppy), Guidewire RFPC-35-145 G07914
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1840-2022·2022-10-05

    Cook Roadrunner PC Guidewire Recalled for Compromised Packaging Seal

    Cook Incorporated recalls Roadrunner PC Wire Guide devices due to a potential packaging seal breach that may compromise sterility. The recall affects 115 units distributed domestically and internationally.

    Product
    Roadrunner PC Wire Guide (The Firm LT), Guidewire Reference Part Number/GPN RLPC-35-145 G06866
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V741000·2022-10-05

    2023 BMW iX Transmission Defect Risk of Vehicle Rollaway

    BMW is recalling one 2023 iX with a defective transmission final drive gear weld that could break, causing vehicle rollaway if the parking brake is not engaged. Dealers will replace the electric drive unit at no cost.

    Product
    BMW — BMW IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1826-2022·2022-10-05

    Bentson Wire Guide Devices Recalled for Potential Sterility Compromise

    Cook Incorporated is recalling Bentson Wire Guide devices due to potential packaging defects that may compromise device sterility.

    Product
    Bentson Wire Guide, Guidewire (OUS ONLY); Reference Part Number: TSMB-35-145 (GPN G27041)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1831-2022·2022-10-05

    Cook Medical Wire Guide Devices Recalled for Packaging Breach

    Cook Incorporated is recalling specific lots of Double Flexible Tipped Wire Guide Guidewire devices due to a complete breach of the packaging chevron seal, which may compromise sterility.

    Product
    Double Flexible Tipped Wire Guide, Guidewire Reference Part Number/GPN TDOC-35-145-0-3 G00362 C-TDOC-18-50-0-2 G05146 TDOC-35-50-0-3 G00364 C-DOC-21-40-0-2 G02431 C-TDOC-21-50-0-2 G05195 C-TDOC-25-50-0-2 G05145
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1812-2022·2022-10-05

    t:slim X2 Insulin Pumps Recalled for Software Issues Affecting Blood Sugar Management

    Tandem Diabetes Care is recalling approximately 8,399 t:slim X2 insulin pumps due to software malfunctions that may affect blood sugar control. A software update is available to resolve the issues.

    Product
    t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim x2 insulin pump with the Control-IQ Technology
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Food)·F-1792-2022·2022-10-05

    A&W Root Beer Zero Sugar Recalled for Undeclared Sugar Content

    A&W Root Beer Zero Sugar in 20oz bottles is being recalled because it contains full sugar but is labeled as sugar-free. The affected product has lot number 071892 and was distributed in DC, MD, PA, and VA.

    Product
    "A&W Root Beer Zero Sugar" packaged in 20oz PET bottles. UPC: 00-0-78000-05340-1
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1785-2022·2022-10-05

    BD Pyxis MedBank Cabinet Software Update Prevents Drawer Access

    A software update for BD Pyxis MedBank medication dispensing cabinets contains an incompatible file that prevents Matrix drawers from opening, potentially delaying medication access in healthcare facilities.

    Product
    BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 . MedBank 200 Main operating with Windows 7 . MedBank 500 Main operating with Windows 7. An automated dispensing cabinet…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1854-2022·2022-10-05

    Barco Medical Network Adapter Recalled for Installation Issues

    Barco NV recalls 169 NexxisOR system network adapters (models K9303078A and K9303097A) due to installation issues. The affected devices were distributed in Florida, Illinois, and New Jersey.

    Product
    Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A
    Category
    Medical Device
    Distribution
    Distributed nationwide