The Recall Desk

State

Massachusetts product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37976–38000 of 82058

  • HighFDA (Devices)·Z-1209-2019·2019-05-01

    Fresenius Kabi CATSmart Autotransfusion Device Recalled for Tubing Wear Risk

    Fresenius Kabi is recalling 342 CATSmart autotransfusion devices because tubing may contact the washing chamber, causing wear or puncture.

    Product
    Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and kits (9005104 AT-1 Autotransfusion set, 9108504 ATF 120 Fast Start Kit, and 9108494 ATF 40 Fast Start Kits); 2. AT-3 Autotransfusion sets and kits…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1298-2019·2019-05-01

    Patagonia Provisions Chipotle Lime Savory Seeds Recalled for Gluten Contamination

    Patagonia Provisions is recalling Chipotle Lime Savory Seeds labeled as gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Chipotle Lime Savory Seeds; 1 oz. poly-film pouches. 12 pouches per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2019·2019-05-01

    Brainlab RT Elements Software Recalled for Incorrect Dose Calculation

    Brainlab AG is recalling specific versions of RT Elements software due to a potential for incorrect dose distribution calculations when using the Pencil Beam algorithm on the GPU.

    Product
    RT Elements Software revisions of the RT Elements applications have a specific software version number. Specifically the following RT Elements applications/versions are affected: - Cranial SRS 1.0.0 and 1.5.0 - Spine SRS 1.0.0 and 1.5.0 - Multiple Brain Mets SRS 1.5.0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1305-2019·2019-05-01

    Mineralife Trace Minerals Dietary Supplement Recalled for Pseudomonas Contamination

    Mineralife LLC is recalling Trace Minerals Dietary Supplement bottles due to potential contamination with Pseudomonas aeruginosa.

    Product
    Trace Minerals Dietary Supplement , 16.2 fl oz (480 mL) bottles, Packaged in dark blue plastic bottles, For freshness, keep refrigerated after opening
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·19113·2019-05-01

    DAVIDsTEA Recalls Valentine's Day Stackable Mugs Due to Fire Hazard

    DAVIDsTEA is recalling about 700 Valentine's Day stackable mugs because they were mislabeled as microwave safe, posing a fire hazard if used in a microwave.

    Product
    Valentine's Day stackable mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1204-2019·2019-05-01

    Siemens Digital Linear Accelerators Recalled for Motion Protection Safety Advisory

    Siemens Medical Solutions USA is recalling 120 digital linear accelerators nationwide to prevent patient or user injury from disabling the Automatic Motion Protection function.

    Product
    Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON M2/Primus Mid-Energy PRIMUS PRIMUS HI ONCOR Impression ONCOR Impression Plus ONCOR Avant Garde ONCOR Expression ARTISTE, ONCOR, and PRIMUS running the following: Control Console from software…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V339000·2019-05-01

    Indian Recalls 2014 Chief and Chieftain Motorcycles for Lighting Defect

    Indian Motorcycle is recalling 2014 Chief and Chieftain models because a Vehicle Control Module issue may cause all front lights to go out, increasing crash risk.

    Product
    INDIAN — INDIAN CHIEF CLASSIC, CHIEFTAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1222-2019·2019-05-01

    Ortho-Clinical Diagnostics Recalls VITROS XT 7600 Systems Due to Software Error

    Ortho-Clinical Diagnostics is recalling 80 VITROS XT 7600 Integrated Systems because a software error may cause incorrect test results without alerting the user.

    Product
    VITROS XT 7600 Integrated System, Product Code 6844461, UDI 1075870031658 Product Usage: The VITROS XT 7600 Integrated System is intended for use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1299-2019·2019-05-01

    Patagonia Provisions Savory Seeds Recalled for Gluten Contamination

    Patagonia Provisions is recalling Savory Seeds Variety Packs labeled gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Savory Seeds Variety Pack; Classic Barbecue, Chipolte Lime, Mellow Curry 1 oz. poly-film pouches, 12 packages per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V340000·2019-05-01

    PACCAR Recalls 2020 Peterbilt and Kenworth Trucks for Mirror Defect

    PACCAR is recalling 2020 Peterbilt and Kenworth trucks because mirror glass may detach, creating a road hazard and reducing driver visibility.

    Product
    PETERBILT — PETERBILT, KENWORTH 567, 579, T680, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2019·2019-05-01

    Thoratec HeartMate 3 Coring Tool Recalled for Foreign Particle Contamination

    Thoratec Corp. is recalling HeartMate 3 Coring Tools because a small black plastic particle was observed in a patient's left ventricle during an implant procedure.

    Product
    Thoratec HeartMate 3 Coring Tool, Sterile EO, Rx Only, REF 10005872, an optional accessory of Thoratec HeartMate 3 Left Ventricular Assist System - Product Usage: The HeartMate 3 Coring Tool is intended for use with the HeartMate 3 Left Ventricular Assist System (LVAS). The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2019·2019-05-01

    Arthrex Burr Recalled for Excessive Heat Generation During Use

    Arthrex, Inc. is recalling specific lots of Arthrex Oval Burr devices because they may generate excessive heat during use, posing a risk of injury to patients.

    Product
    Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous tissues in both large and small articular cavities during arthroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1215-2019·2019-05-01

    Stryker Performance Series Sagittal Blade Recall for Sterility Breach

    Stryker is recalling 355 Performance Series Sagittal Blades due to a potential breach in sterility caused by improper packaging positioning during manufacture.

    Product
    Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades are used in the cutting and shaping of bone and other bone related tissue in various orthopedic procedures. Typical procedures include, total-knee…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1218-2019·2019-05-01

    Jelco ViaValve Safety Intravenous Catheters Recalled for Manufacturing Defect

    Smiths Medical ASD Inc. is recalling specific lots of Jelco ViaValve safety intravenous catheters due to a V-shaped puncture at the base of the catheter.

    Product
    Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters, 18G x 1 1/4", Model Number REF 3265, MOD 10 The Jelco(R) ViaValve(TM) safety I.V. catheter is a sterile, non pyrogenic, single use, radiopaque intravascular catheter device used for the administration of medically…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1207-2019·2019-05-01

    Carestream OnSight 3D Extremity System Recalled for Software Data Error

    Carestream Health is recalling 37 OnSight 3D Extremity Systems because a software error may leave companion imaging volumes in the original patient's exam during re-assignment.

    Product
    OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574 (w/ Remote Console) The device is intended to be used for x-ray computed tomography and projection x-ray imaging of upper and lower extremities of adult…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1213-2019·2019-05-01

    Covidien Procedure Kits Recalled for Sterilization Labeling Inconsistency

    Covidien LLC is recalling 148 procedure kits because the sterilization method used was not consistent with the labeling and approved method.

    Product
    Procedure kits include devices from the affected lots distributed OUS only: (1)BOX KIT00529H KIT COLECISTECTOMIA ACCESO (2)BOX KIT00680 KIT COLECISTECTOMIA- (3)BOX KIT00681 KIT APENDICECTOMIA (4)BOX KIT00897 KIT COLON IZQUIERDO (5)BOX LAPL1 ZESTAW DO CHOLECYSTEKTOMII…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1220-2019·2019-05-01

    Abbott Recalls 32 St. Jude Medical Confirm Rx Insertable Cardiac Monitors

    Abbott is recalling 32 St. Jude Medical Confirm Rx Insertable Cardiac Monitors because the devices incorrectly determine that their security certificates have expired, preventing them from pairing with the mobile app.

    Product
    St. Jude Medical Confirm Rx Insertable Cardiac Monitor, REF DM3500, Sterile. Product Usage: The St. Jude Medical Confirm Rx insertable cardiac monitor (ICM) is designed to detect arrhythmias and wirelessly transmit data to the Merlin.net Patient Care Network (PCN). It is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1296-2019·2019-05-01

    Patagonia Provisions Classic Barbecue Savory Seeds Recalled for Gluten Contamination

    Patagonia Provisions is recalling Classic Barbecue Savory Seeds labeled gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Classic Barbecue Savory Seeds; 1 oz. poly-film pouches. 12 units per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1212-2019·2019-05-01

    Covidien Endo Grasp Auto Suture Grasper Recalled for Sterilization Labeling Error

    COVIDIEN LLC is recalling 240 units of the Endo Grasp Auto Suture Grasper 5mm because the sterilization method used was not consistent with the labeling and approved method.

    Product
    Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Covidien Endo Grasp" Auto Suture" grasper 5 mm instrument has applications in a variety of gynecologic, general, urologic, thoracic and endoscopic procedures for temporary grasping/clamping of tissue and small…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1208-2019·2019-05-01

    Exactech Recalls Mismarked Truliant Tibial Fit Trays for Knee Replacement

    Exactech is recalling 18 Truliant Tibial Fit Trays because they were mismarked as size 3. The devices were distributed to facilities in 10 US states.

    Product
    Truliant Tibial Fit Tray Cemented SZ 3F / 3T, Catalog Number 02-022-45-3030 Product Usage: Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented The OPTETRAK Comprehensive Knee Systems are indicated for use in skeletally mature individuals undergoing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1302-2019·2019-05-01

    Mediterranean Brands Callaloo Greens Recalled for Potential Plastic Contamination

    American Pasteurization Company is recalling Mediterranean Brands Callaloo Greens due to potential contamination with plastic foreign material.

    Product
    Mediterranean Brands Callaloo Greens, Product 6017. Net Weight 15.0 lbs (6.90 Kgs). Keep Frozen. Manufactured for: MBI, Glenview, IL 60025
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1297-2019·2019-05-01

    Patagonia Provisions Mellow Curry Savory Seeds Recalled for Gluten

    Patagonia Provisions is recalling Mellow Curry Savory Seeds labeled gluten-free because they contain gluten in excess of 20 ppm.

    Product
    Patagonia Provisions Mellow Curry Savory Seeds; 1 oz. poly-film pouches. 12 pouches per case Vegan, Gluten Free Distributed by Patagonia Provisions, Inc. Sausalito, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1221-2019·2019-05-01

    Maquet Edi Catheter Recalled for Incorrect Expiry Date Labeling

    Getinge is recalling Maquet Edi Catheters because the single-pack boxes are labeled with the wrong expiry date. The recall covers 17 boxes distributed in the US and several countries.

    Product
    Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg Product Code/REF Number: 6685775 Product Usage: The Edi Catheter is a single-use naso-gastric feeding tube with an electrode array of ten electrodes. The Edi Catheter is intended for: - Detecting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1241-2019·2019-05-01

    Akorn Recalls Fentanyl Citrate Injection Due to Impurity Specification Failure

    Akorn Inc. is recalling Fentanyl Citrate Injection, USP, 100 mcg/2 mL, because it failed impurity specifications during stability testing.

    Product
    Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-25
    Category
    Drug
    Distribution
    Distributed nationwide