The Recall Desk

State

Maryland product recalls

73,219 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
2,134
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 2,134 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,224 recalls whose distribution notice names Maryland specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15901–15925 of 81443

  • SevereFDA (Devices)·Z-2374-2023·2023-08-23

    Dialysis Catheter Recall: Center Lumen Occlusion Due to Excessive Lubricant

    Covidien LP is recalling MAHURKAR 12 Fr dialysis catheters due to center lumen occlusion from excessive lubricant. The defect may cause treatment delays and serious complications including embolism and thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, PASS Tray REF: 8888103002HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2390-2023·2023-08-23

    Dialysis Catheter Occlusion Recall Due to Excessive Lubricant Coating

    Covidien recalls 647 MAHURKAR dialysis catheters due to center lumen occlusion caused by excessive silicone lubricant. The blockage may delay treatment or increase risks of blood clots.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, Kit REF: 8888345637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2386-2023·2023-08-23

    MAHURKAR dialysis catheters recalled for center lumen occlusion risk

    Covidien LP recalls MAHURKAR dialysis catheters due to excessive silicone lubricant on the catheter tip, which can obstruct the center lumen. This may delay treatment and cause serious blood complications including embolism and thrombosis.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, Kit" REF: 8888345611
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2378-2023·2023-08-23

    Dialysis catheter recall: excessive lubricant causes center lumen obstruction

    A dialysis catheter product is being recalled due to excessive lubricant coating in the center lumen, which may cause full or partial obstruction. The blockage could delay treatment and increase risk of blood clots and hemolysis.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2369-2023·2023-08-23

    Dialysis Catheter Recalled Due to Silicone Lubricant Obstruction Risk

    Covidien LP is recalling 5,373 MAHURKAR dialysis catheters because excessive silicone lubricant can occlude the catheter lumen, potentially causing treatment delays or blood clotting complications.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, IC Tray REF: 8888101003HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2389-2023·2023-08-23

    MAHURKAR Dialysis Catheter Recalled for Center Lumen Obstruction Risk

    Covidien LP recalled 15,209 MAHURKAR dialysis catheters due to excessive lubricant in the center lumen, which may cause catheter occlusion, reduce blood flow, or lead to hemolysis and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2385-2023·2023-08-23

    Acute Dialysis Catheter Recalled for Potential Lumen Obstruction and Embolism Risk

    Covidien is recalling MAHURKAR acute dialysis catheters for excessive silicone lubricant causing lumen obstruction that may delay treatment and lead to hemolysis, embolism, or thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit REF: 8888345603HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2380-2023·2023-08-23

    FDA Recalls Mahurkar Dialysis Catheter for Potential Tip Obstruction Risk

    Covidien's Mahurkar acute dialysis catheters may have excessive silicone lubricant causing tip obstruction. This could delay treatment or cause serious complications including blood clots and embolism.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, Kit REF: 8888340637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2384-2023·2023-08-23

    Dialysis catheters recalled for potential center lumen obstruction

    Covidien LP is recalling MAHURKAR dialysis catheters because excessive silicone lubricant coats the center lumen, potentially blocking blood flow or creating clots and other blood vessel complications.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit" REF: 8888345603
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2368-2023·2023-08-23

    Dialysis Catheter Recalled Due to Excessive Lubricant Causing Center Lumen Obstruction

    Covidien is recalling MAHURKAR dialysis catheters due to excessive silicone-based lubricant coating the center lumen tip, which may cause partial or complete obstruction, delaying treatment or causing thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, IC Tray REF: 8888101002HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2375-2023·2023-08-23

    Dialysis catheter recalled due to excessive lubricant causing obstruction

    Covidien's MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can block the center lumen, preventing or reducing blood flow during dialysis. This Class I recall affects 271 units and carries risk of treatment delays, hemolysis, and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, PASS Tray REF: 8888103004HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1440-2023·2023-08-23

    Trader Joe's Joe-Joe's Cookies Recalled for Undeclared Peanut Allergen

    Commercial Bakeries is recalling Trader Joe's Joe-Joe's Chocolate Vanilla Creme cookies due to undeclared peanut allergen. Consumers with peanut allergies should not consume this product and should return it to the store.

    Product
    Trader Joe's Joe-Joe's Chocolate Vanilla Creme Flavored With Other Natural Flavors Net Wt.13.4 oz (380g) UPC: 0076 5725 Packaged in trays. 26 units per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2414-2023·2023-08-23

    FreeStyle Libre 2 Readers may fail to activate new sensors

    FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.

    Product
    FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1448-2023·2023-08-23

    Frozen Sachertote Recalled for Undeclared Egg, Milk, and Wheat Allergens

    Lidl US TRADING is recalling Alpenfest Style Sachertote frozen dessert because egg, milk, and wheat allergens are not declared on the label. Consumers with allergies to these ingredients should not consume the product.

    Product
    Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2413-2023·2023-08-23

    HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard

    Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.

    Product
    HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1437-2023·2023-08-23

    Pumpkin Creme Cookies Recalled Due to Undeclared Peanut Allergen

    Commercial Bakeries is recalling Ruxton Chocolates Manning Brand Pumpkin Creme Cookies because the product contains undeclared peanut. The recall affects 4834 cases distributed to retail locations in IL, NJ, MD, NY, CT, CA, and FL.

    Product
    Ruxton Chocolates Manning Brand Pumpkin Creme Cookies 19.5 oz. Bulk product packaged in bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-1084-2023·2023-08-23

    Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons

    Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.

    Product
    hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1434-2023·2023-08-23

    Benton's Snack Packs Recalled for Undeclared Peanut Allergen

    Benton's 100 Calorie Snack Packs are recalled because they contain undeclared peanut, a major allergen. Consumers with peanut allergies may experience severe reactions if they consume this product.

    Product
    Benton's 100 Calorie Snack Packs Baked Chocolate Wafer Snacks 6-0.81 OZ (23g) Packs Net Wt. 4.86 oz UPC: 4 099100 040416 Packaged in a paper carton, 16 cartons per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1436-2023·2023-08-23

    Gluten Free MI-DEL Swedish Style Ginger Snaps recalled for undeclared peanut

    Gluten Free MI-DEL Swedish Style Ginger Snaps (8 oz and 10 oz packages) are being recalled because they contain undeclared peanut. Consumers with peanut allergies should not consume this product and should return it to the retailer or dispose of it safely.

    Product
    Gluten Free MI-DEL Swedish Style Ginger Snaps Net Wt. 8 oz (227g) & 10 oz UPC:3068476890. Packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1441-2023·2023-08-23

    Ginger Snap Cookies Recalled for Undeclared Peanut Allergen

    Simply MI-Delicious Swedish Style Ginger Snaps are recalled due to undeclared peanut. People with peanut allergies are at risk.

    Product
    Simply MI-Delicious MI-DEL Swedish Style Ginger Snaps Net Wt. 10 oz (284g)UPC:3068403502. Packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighNHTSA·23V592000·2023-08-23

    Bentley Recalls 2017-2023 Bentayga Vehicles for Fuel Leak Fire Risk

    Bentley is recalling 2017-2023 Bentayga vehicles because fuel supply module wiring can overheat, melt a flange, and cause a fuel leak that increases fire risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2401-2023·2023-08-23

    UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage

    Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.

    Product
    UroPass Ureteral Access Sheaths, 5 pieces/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1435-2023·2023-08-23

    Annie's Homegrown Graham Snack Recalled for Undeclared Peanut

    Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla 6.75 oz boxes are recalled due to undeclared peanut. Consumers with peanut allergies should not consume this product.

    Product
    Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla Flavored With Other Natural Flavors Graham-Style Snacks Net Wt 6.75 oz (191g) UPC: 13562 00019 Packaged in cartons, 7 and 12 retails cartons per case
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2405-2023·2023-08-23

    Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm

    Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.

    Product
    CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide