The Recall Desk

State

Massachusetts product recalls

73,824 recalls have nationwide distribution and so reach Massachusetts. 8,252 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total
8,252
Critical
1,179
Severe
2,360
Most recent
2026-11-04

Of the 8,252 recalls naming Massachusetts we have scored against our rubric, 1,179 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,360 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44601–44625 of 82076

  • ModerateFDA (Drugs)·D-0542-2018·2018-02-14

    Teva Recalls Fentanyl Transdermal Systems Due to Impurity Levels

    Teva Pharmaceuticals is recalling specific lots of Fentanyl Transdermal Systems because they contain a degradant called Fentanyl-n-Oxide that exceeds safety limits.

    Product
    Fentanyl Transdermal System. 75 mcg/h, packaged in 5 pouch system (NDC 0591-3213-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3213-54.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0809-2018·2018-02-14

    Bobo's Coconut Oat Bars Recalled Due to Mold Contamination

    Simply Delicious, Inc. is recalling Bobo's Coconut Oat Bars because they may contain mold. The recall covers 588 master cases distributed nationwide.

    Product
    Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per single bar
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0526-2018·2018-02-14

    Angiodynamics Recalls Accu2i pMTA Microwave Tissue Ablation Applicators

    Angiodynamics, Inc. is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering desired microwave energy.

    Product
    Accu2i pMTA Applicator, 14 cm STANDARD, REF/Catalog # 900-600, Model # (UPN) H7879006000, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the intraoperative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0549-2018·2018-02-14

    Zimmer Biomet Recalls Humeral Guide Wire Ball Tip Due to Packaging Design Verification

    Zimmer Biomet is recalling 7,888 Humeral Guide Wire Ball Tip units because the previous packaging configuration lacks design verification for 70cm wires.

    Product
    Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length, Item Number 47-2255-008-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during implantation. The guide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0250-2018·2018-02-14

    G & W Laboratories Recalls Ciclopirox Olamine Cream Due to Discoloration

    G & W Laboratories is recalling 142,236 tubes of Ciclopirox Olamine Cream USP, 0.77%, due to yellow discoloration. The product is distributed nationwide and in Puerto Rico.

    Product
    CICLOPIROX OLAMINE — CICLOPIROX OLAMINE (CICLOPIROX OLAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0541-2018·2018-02-14

    Teva Recalls Fentanyl Patches Due to Impurity Exceeding Limits

    Teva Pharmaceuticals is recalling Fentanyl Transdermal Systems because a degradation product exceeded safety limits.

    Product
    Fentanyl Transdermal System, 50 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3212-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3212-54.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0543-2018·2018-02-14

    Teva Recalls Fentanyl Transdermal Systems Due to Impurity Exceeding Limits

    Teva Pharmaceuticals is recalling specific lots of Fentanyl Transdermal Systems because a degradation product exceeded safety limits.

    Product
    Fentanyl Transdermal System, 100 mcg/h, packaged in 5 pouch system (NDC 0591-3214-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3214-54.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18097·2018-02-13

    Tea Collection Recalls Children's Rompers Due to Choking Hazard

    Tea Collection is recalling about 3,800 children's rompers because snaps near the collar can detach, posing a choking hazard to young children.

    Product
    Children's rompers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowNHTSA·18V105000·2018-02-13

    Gulf Stream Recalls 2018 Matrix and Geo Trailers for Label Errors

    Gulf Stream is recalling 2018 Matrix and Geo recreational trailers because the Federal Certification Labels incorrectly list the rear axle weight rating.

    Product
    GULF STREAM — GULF STREAM MATRIX, GEO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V104000·2018-02-12

    Ford Recalls 2018 Escape and Lincoln MKC for Brake Hose Defect

    Ford is recalling 2018 Escape and Lincoln MKC vehicles because incorrect front brake hoses may chafe and leak fluid, increasing stopping distance.

    Product
    LINCOLN — LINCOLN, FORD MKC, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V103000·2018-02-09

    Mitsubishi Recalls Outlander Sport for Wiper Link Corrosion Risk

    Mitsubishi is recalling 2011-2016 Outlander Sport vehicles because water intrusion may corrode the wiper link, causing wipers to stop working and reducing visibility.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V102000·2018-02-09

    Volkswagen Recalls 2017-2018 Tiguan Limited for Incorrect Front Driver Air Bag

    Volkswagen is recalling 2017-2018 Tiguan Limited vehicles because the front driver air bag may not be intended for US use, failing federal safety standards and increasing injury risk in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18096·2018-02-08

    Fujitsu Recalls Notebook Computer Battery Packs Due to Fire and Burn Hazards

    Fujitsu is recalling specific lithium-ion battery packs for notebook computers and workstations because they can overheat, posing fire and burn risks.

    Product
    Battery packs used in Fujitsu notebook computers and workstations.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V101000·2018-02-08

    Micro Bird Recalls T-Series Transit Buses Due to Seat Belt Anchor Defect

    Micro Bird is recalling 2015-2018 T-Series transit buses because seat belt attachments may not remain secured to the floor in a crash, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18723·2018-02-08

    Poppin Recalls Pitch Rolling Chairs Due to Fall Hazard

    Poppin is recalling about 2,800 Pitch rolling chairs because the seat plate can break and detach, posing a fall hazard. No injuries have been reported.

    Product
    Pitch rolling chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V098000·2018-02-08

    Chrysler Recalls 2017 Jeep Wrangler and Dodge Caravan for Brake Switch Defect

    Chrysler is recalling 2017 Jeep Wrangler and Dodge Caravan vehicles because brake switches may malfunction, allowing the vehicle to shift out of Park without the brake pedal being pressed.

    Product
    JEEP — JEEP, DODGE WRANGLER, CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18095·2018-02-08

    Husqvarna Recalls Zero Turn Riding Mowers Due to Fire Hazard

    Husqvarna is recalling about 7,100 residential zero turn riding mowers because a fuel line defect can cause leaks and fire. No injuries have been reported.

    Product
    Residential zero turn riding mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V100000·2018-02-08

    RAM Trucks Recalled for Transmission Shift Interlock Defect

    Chrysler is recalling 2017-2018 RAM trucks because the brake pedal interlock may fail, allowing the vehicle to shift out of Park without the brake pedal being pressed.

    Product
    RAM — RAM 2500, 5500, 1500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0247-2018·2018-02-07

    Blue Pearl Capsules Recalled for Undeclared Sildenafil

    Blue Fusion Natural is recalling Blue Pearl capsules because FDA analysis found undeclared sildenafil, an unapproved drug for erectile dysfunction.

    Product
    BLUE PEARL capsules, 500mg, 1-count packets, Distributed by Blue Pearl Long Beach, CA UPC 8 4704600978 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0472-2018·2018-02-07

    Clopidogrel Tablets Recalled Due to Simvastatin Labeling Error

    International Laboratories, LLC is recalling Clopidogrel Tablets 75 mg because bottles were found containing Simvastatin Tablets 10 mg.

    Product
    Clopidogrel Tablets, USP 75 mg, 30-count bottles, Rx only, Packaged for: International Laboratories, LLC St. Petersburg, FL 33710, NDC 54458-888-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0267-2018·2018-02-07

    Medline Incision and Drainage Tray Kit Recalled for Subpotent Iodine

    Medline is recalling Incision and Drainage Tray Kits because the Povidone-Iodine prep pads contain less iodine than labeled.

    Product
    Medline Incision and Drainage Tray Kit, Sterile, Single use only. Packaged in USA for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0306-2018·2018-02-07

    Medline Anesthesia Kit Recalled for Subpotent Povidone-Iodine Concentration

    Medline Industries is recalling 60 cases of Anesthesia Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.

    Product
    Medline Anesthesia Kit, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Northfield, IL 60093
    Category
    Drug
    Distribution
    Distributed nationwide