The Recall Desk

State

Maine product recalls

72,907 recalls have nationwide distribution and so reach Maine. 3,894 additional recalls listed Maine specifically in their distribution scope.

What the numbers show

Total
3,894
Critical
468
Severe
791
Most recent
2026-09-02

Of the 3,894 recalls naming Maine we have scored against our rubric, 468 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 791 (20%) are Severe.

These figures cover only the 3,894 recalls whose distribution notice names Maine specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1376–1400 of 76801

  • SevereCPSC·26550·2026-06-11

    Kawasaki Teryx4 and Teryx5 H2 drive converter sheaves can break

    About 3,585 model year 2026 Kawasaki Teryx4 H2 and Teryx5 H2 off-road vehicles are being recalled after 19 reports of drive converter sheave breakage.

    Product
    Model Year 2026 Teryx4 H2 and Teryx5 H2 recreational off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V384000·2026-06-11

    Altec Recalls AC Series Cranes Due to Missing Welds on Jib

    Altec Industries is recalling 2024-2026 AC Series Cranes because missing welds on the 26-foot insulating personnel jib may cause the platform to fall, increasing injury risk.

    Product
    ALTEC — ALTEC AC SERIES CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26555·2026-06-11

    Houoto pool drain covers lack required markings under federal law

    About 595 Houoto 642-2150V pool drain covers are being recalled because they lack required product markings under the Virginia Graeme Baker Pool and Spa Safety Act.

    Product
    Houoto 642-2150V Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26536·2026-06-11

    Sloosh dive sticks violate federal ban and pose impalement hazard

    About 254,000 Sloosh dive sticks, sold in packages of Sloosh water toys model 40041, are being recalled because they exceed the compress limit under the federal dive sticks ban.

    Product
    Sloosh Dive Sticks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2212-2026·2026-06-10

    Pediatric care bed KayserBett IDA recalled due to entrapment hazard

    KayserBett IDA pediatric care beds are being recalled because the hand control can be operated by children, creating a risk of entrapment and serious injury or death.

    Product
    Pediatric care bed; Product Designation: KayserBett IDA;
    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-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-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
  • 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 (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-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-2252-2026·2026-06-10

    BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2257-2026·2026-06-10

    BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are 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: 405637, 405707.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2249-2026·2026-06-10

    BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke 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: 405621, 405735.
    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