The Recall Desk

State

Maine product recalls

20,364 recalls have nationwide distribution and so reach Maine. 0 additional recalls listed Maine specifically in their distribution scope.

About recalls in Maine

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Maine consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

13876–13900 of 20364

  • HighFDA (Drugs)·D-0458-2023·2023-03-22

    Alprazolam Tablets Recalled for Potential Cross-Contamination Risk

    Breckenridge Pharmaceuticals is recalling Alprazolam Tablets, USP 0.25mg distributed nationwide due to a potential cross-contamination risk from manufacturing deviations.

    Product
    Alprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01), b) 500-count bottle and c) 1,000-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berli
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0608-2023·2023-03-22

    Sunflower Lecithin Liquid Products Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling sunflower lecithin liquid in bulk totes due to undeclared peanut allergen. The affected products were distributed nationwide to food manufacturers.

    Product
    Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.) totes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1258-2023·2023-03-22

    Dimension Tacrolimus Diagnostic Cartridge Recalled for Measurement Imprecision

    Siemens is recalling Dimension Tacrolimus diagnostic test cartridges (lots GA2286, GA3047, GA3171) due to confirmed measurement imprecision that could lead to incorrect drug dosing and potential organ failure or toxicity.

    Product
    Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test for the quantitative measurement of tacrolimus in human whole blood on the Dimension¿ clinical chemistry system SMN: 10700795 (DF207)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0582-2023·2023-03-22

    Pingo Hot Chocolate Pods Recalled for Undeclared Peanut Residue

    Pingo hot chocolate pods may contain undeclared peanut residue. Consumers with peanut allergies should not consume affected products.

    Product
    Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 Count UPC: 810683028150 Pingo Hot Chocolate Pods Variety Pack, 100 Count UPC: 810683029805 Pingo Hot Ch
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1242-2023·2023-03-22

    BD Insulin Syringes Recalled for Nonsterile Condition and Infection Risk

    Becton Dickinson is recalling 686,500 units of BD insulin syringes due to a nonsterile condition that may expose patients to pathogenic microorganisms and risk of infection.

    Product
    BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1244-2023·2023-03-22

    BD Ultra-Fine II insulin syringes recalled for sterility defect

    Becton Dickinson recalled 1,472,400 BD Ultra-Fine II insulin syringes due to a sterility defect. The nonsterile syringes pose a risk of local infection at injection sites.

    Product
    BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326725
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1245-2023·2023-03-22

    Fusion Bioline Vascular Graft recalled due to manufacturing straightness defect

    Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.

    Product
    Fusion Bioline Vascular Graft, Part number M00201503046B0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0459-2023·2023-03-22

    Alprazolam Tablets Recalled Due to Potential Cross-Contamination Risk

    Breckenridge Pharmaceutical is recalling multiple lots of Alprazolam 0.5mg tablets nationwide due to manufacturing process deviations that created a potential cross-contamination risk.

    Product
    Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: B
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0580-2023·2023-03-22

    Two Rivers Coffee pods recalled for undeclared peanut residue

    Two Rivers Coffee hot cocoa pods in variety packs may contain undeclared peanut residue. Consumers with peanut allergies should not consume these products and should check the affected product codes.

    Product
    Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection packaged in single serve pods. Pods are packaged in the following Two Rivers Variety Pack boxes: -Two Rivers Coffee Hot Cocoa Pods, Single Serve Variety Sampler Pack , 40 Count UPC: 810683022554 -Two Rivers Coffee Hot C
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0465-2023·2023-03-22

    Buprenorphine Transdermal System Recalled for Failed Impurity Specifications

    AVEVA Drug Delivery Systems recalls nationwide batches of Buprenorphine Transdermal patches due to a degradation impurity exceeding acceptable limits during stability testing.

    Product
    Buprenorphine Transdermal System, CIII 10 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7077-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0462-2023·2023-03-22

    Clobazam tablets recalled for potential manufacturing cross-contamination risk

    Breckenridge Pharmaceuticals is recalling certain lots of Clobazam 10 mg tablets due to a potential cross-contamination risk stemming from manufacturing process deviations.

    Product
    Clobazam Tablets, 10 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-900-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0609-2023·2023-03-22

    Organic Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling Organic Sunflower Lecithin Powder (44 lb boxes) due to undeclared peanut allergen. The product was distributed to a distributor in Missouri and then nationwide to manufacturers.

    Product
    Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0466-2023·2023-03-22

    Buprenorphine Transdermal System 20 mcg/hour Recalled for Specification Failure

    AVEVA Drug Delivery Systems recalls Buprenorphine Transdermal System 20 mcg/hour (Lot 51836) nationwide due to degradation product impurity exceeding specification limits during stability testing.

    Product
    Buprenorphine Transdermal System, CIII 20 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7079-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0464-2023·2023-03-22

    Evamist (Estradiol) Transdermal Spray Recalled for Failed Content Uniformity

    Padagis US LLC is recalling 43,238 cartons of Evamist (Estradiol) transdermal spray nationwide because the spray content uniformity specification for standard deviation was not met at the 18-month stability time point.

    Product
    EVAMIST — EVAMIST (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2023·2023-03-22

    In Vitro Diagnostic GI Panel Recalled Due to Temperature Exposure During Shipping

    BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.

    Product
    In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - REF RFIT-ASY-0116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1252-2023·2023-03-22

    BioFire Respiratory Panel 2.1 Recalled Due to Temperature Shipping Excursions

    BioFire Diagnostics is recalling BioFire Respiratory Panel 2.1 (RP2.1) diagnostic kits due to temperature excursions during shipping that may reduce device performance.

    Product
    In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1) - REF 423742
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1251-2023·2023-03-22

    BioFire BCID2 Diagnostic Panels Recalled for Temperature-Related Performance Issues

    BioFire Diagnostics is recalling BioFire BCID2 diagnostic panels that experienced temperature excursions during shipment, which may reduce their performance. Affected kits were distributed in Florida and Georgia.

    Product
    In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23161·2023-03-17

    Mockingbird Single Strollers Recalled Due to Fall Hazard

    Mockingbird LLC is recalling about 25,390 Single Strollers because the lower side of the frame can crack, posing a fall risk to children. The company is offering a free frame reinforcement kit.

    Product
    Mockingbird Single Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23734·2023-03-16

    Polaris Sportsman ATVs Recalled for Fire and Brake Loss Hazards

    Polaris is recalling model years 2021–2023 Sportsman 450 and 570 ATVs because an improperly assembled wiring harness can contact the brake line and vehicle frame, resulting in front brake loss and fire.

    Product
    Model Years 2021-2023 Sportsman 450 and 570 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23154·2023-03-16

    Pfizer Recalls Nurtec ODT Prescription Tablets for Non-Child-Resistant Packaging

    Pfizer is recalling Nurtec® ODT (rimegepant) 75mg tablets because the blister card packaging is not child-resistant as required by law, posing a poisoning risk to children who may access and swallow the contents.

    Product
    Nurtec® ODT (rimegepant) orally disintegrating tablets, 75mg 8-Unit Dose blister pack
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·23156·2023-03-16

    Fredericksburg Farms 10-Ounce Scented Candles Recalled for Laceration Hazard

    Fredericksburg Farms is recalling about 6,500 scented candles with glass lids because some lids are too tight, causing jars to break when forcibly opened. The company has received four reports of hand lacerations.

    Product
    Fredericksburg Farms 10 Ounce Scented Candles with Glass Lids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23155·2023-03-16

    Ecoxall Sodium and Potassium Hydroxide Products Recalled for Non-Compliant Packaging

    Ecoxall is recalling sodium hydroxide and potassium hydroxide products sold on Amazon because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act. The products pose a risk of chemical burns and skin or eye irritation.

    Product
    Ecoxall Sodium and Potassium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23158·2023-03-16

    STIHL Docking Stations for iMOW Robotic Mowers Recalled for Fire Hazard

    STIHL is recalling about 2,700 iMOW docking stations that can short-circuit when exposed to moisture, creating a fire hazard. Eight reports of thermal overheating and two fires have been reported; no injuries.

    Product
    STIHL docking stations sold with STIHL iMOW® robotic lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23159·2023-03-16

    IKEA LETTAN Mirrors Recalled Due to Laceration Hazard

    IKEA is recalling LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration risk. About 22,400 units in the U.S. are affected.

    Product
    IKEA LETTAN Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23157·2023-03-16

    Sunbeam Queen Size Heated Blankets Recalled for Fire and Burn Hazards

    Sunbeam Queen Size Heated Blankets (model 32810027) can overheat, posing fire and burn hazards. The firm has received 13 reports of overheating with no injuries reported. Consumers should stop using them immediately and contact Star Elite for a refund.

    Product
    Sunbeam® Queen Size Heated Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide