The Recall Desk

State

Maryland product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1476–1500 of 81125

  • SevereFDA (Devices)·Z-2250-2026·2026-06-10

    BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0909-2026·2026-06-10

    Alfredo sauce contains dry milk powder recalled over Salmonella

    Alfredo Sauce in 3 lb 7 oz sealed poly bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2255-2026·2026-06-10

    BD Whitacre spinal trays across nine catalog numbers recalled over bupivacaine

    BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2278-2026·2026-06-10

    Design Options spinal trays recalled over Huons bupivacaine quality issues

    Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.

    Product
    Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2256-2026·2026-06-10

    BD spinal trays recalled as a sub-recall of Huons bupivacaine

    BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2223-2026·2026-06-10

    Ivenix pump software may report false battery health and shut down

    The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.

    Product
    LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0903-2026·2026-06-10

    Birch Benders sweet potato pancake and waffle mix contains undeclared egg

    Birch Benders Sweet Potato Pancake and Waffle Mix, 12 oz, is being recalled because of undeclared egg. The recall covers 5,340 cases.

    Product
    Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Devices)·Z-2276-2026·2026-06-10

    B. Braun spinal needle kits recalled over Huons bupivacaine quality issues

    Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.

    Product
    Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2026·2026-06-10

    BD Quincke spinal trays recalled over Huons bupivacaine quality issues

    BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2253-2026·2026-06-10

    BD combined Whitacre and Quincke spinal trays recalled over bupivacaine

    BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0908-2026·2026-06-10

    Aramark cheese sauce contains dry milk powder recalled over Salmonella

    Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2224-2026·2026-06-10

    Ivenix infusion pumps may hide internal damage after being dropped

    Ivenix Infusion System Large Volume Pumps are being recalled because dropping or jarring can loosen the touchscreen input cable, causing random touches or an unresponsive screen.

    Product
    Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Food)·H-0910-2026·2026-06-10

    Cold prep cream sauce contains dry milk recalled for Salmonella

    Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2251-2026·2026-06-10

    BD Whitacre 22G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0907-2026·2026-06-10

    Cheese sauce mixes contain dry milk powder recalled over Salmonella

    Cheese Sauce Mix and Creamier Cheese Sauce Mix are being recalled because they contain a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954924308 3) Creamier Cheese Sauce Mix, 25 lb., packaged in a tied poly bag an
    Category
    Food
    Distribution
    41 states
  • HighFDA (Devices)·Z-2296-2026·2026-06-10

    Avanta administration tube sets may not engage the flow control valve

    Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.

    Product
    Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2290-2026·2026-06-10

    Philips Azurion 7M12 Roadmap Pro may produce unusable dark images

    Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1016-2026·2026-06-10

    Albertsons Waldorf salad does not declare walnut allergen

    Albertsons store-made Ready Meals Salad Waldorf is being recalled because the contains statement does not declare walnut. 82 units are affected.

    Product
    UPC 21163600000 Ready Meals SALAD WALDORF SS This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0963-2026·2026-06-10

    Albertsons raspberry moon cake does not declare almond allergen

    Albertsons store-made Cake Raspberry Moon 8-inch 2-layer is being recalled because the contains statement does not declare almond. 25 units are affected.

    Product
    UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1036-2026·2026-06-10

    Albertsons sesame mandarin salads do not declare almond allergen

    Albertsons store-made sesame and mandarin salads are being recalled because the contains statement does not declare almond. 196 units are affected.

    Product
    UPC 21870200000 KITCHEN SALAD SESAME ASIAN LARGE SS COLD UPC 27817500000 Ready Meals SALAD MANDARIN SESAME NOODLE SS UPC 29326100000 SALAD SESAME MANDARIN FS COLD This is Albertson's store-made item and sold by unit or random weight at point of s
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0988-2026·2026-06-10

    Albertsons 16-inch carving tray does not declare walnut

    An Albertsons store-made 16-inch carving tray is being recalled because the contains statement does not declare walnut. 12 units are affected.

    Product
    UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1037-2026·2026-06-10

    Albertsons turkey poppyseed salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Turkey Poppyseed is being recalled because the contains statement does not declare almond.

    Product
    UPC 29361000000 KITCHEN SALAD TURKEY POPPYSEED SS COLD UPC 29360900000 KITCHEN SALAD TURKEY POPPYSEED FS COLD This is Albertson's store-made item and sold by random at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1033-2026·2026-06-10

    Albertsons nine-inch peach melba pies do not declare almond

    Albertsons store-made Pie Peach Melba 9-inch is being recalled because the contains statement does not declare almond. Seven units are affected.

    Product
    UPC 25688000000 PIE PEACH MELBA 9IN This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1029-2026·2026-06-10

    Albertsons sliced loaf platter does not declare walnut allergen

    Albertsons store-made Platter Loaf Sliced, 20 count, is being recalled because the contains statement does not declare walnut. 20 units are affected.

    Product
    UPC 22650200000 PLATTER LOAF SLC 20CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide