The Recall Desk

State

Massachusetts product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48701–48725 of 82079

  • ModerateFDA (Food)·F-2178-2017·2017-05-10

    Source Naturals Vitamin D-3 Recalled for Lower Concentrations

    Threshold Enterprises Ltd is recalling specific lots of Source Naturals Vitamin D-3 dietary supplements because testing found lower concentrations than labeled.

    Product
    Source Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone and Immune Health 2000 IU per serving, 500% DV. Other ingredients: Vegetable Glycerin, Deionized water, citric acid, Natural orange flavor and lemon essential oil. Use 5 drops once daily in a drink.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1954-2017·2017-05-10

    Anspach Effort SC2100 Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 22 SC2100 foot controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Foot Control without Switches, SC2100 Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2008-2017·2017-05-10

    Anspach Effort Bearing Sleeve Recall for Missing Service Interval

    The Anspach Effort, Inc. is recalling 58 Bearing Sleeve units because the supplied directions for use did not contain a recommended service interval.

    Product
    Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1912-2017·2017-05-10

    Smith & Nephew Recalls Radial Osteotome Blades Due to Stability Data

    Smith & Nephew is recalling specific lots of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0696-2017·2017-05-10

    Akorn Recalls Sulfamethoxazole and Trimethoprim Oral Suspension for Dissolution Failures

    Akorn Inc is recalling 55,968 bottles of Sulfamethoxazole and Trimethoprim Oral Suspension because the product failed to meet dissolution specifications.

    Product
    Sulfamethoxazole and Trimethoprim Oral Suspension, USP 200 mg / 40 mg per 5 mL , Grape Flavor, Rx Only, 16 fl oz. (473 mL), HI-TECH PHARMACAL CO., INIC, Amityville, NY 11701, NDC 50383-824-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2000-2017·2017-05-10

    Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 10.5cm Long Attachments for pneumatic systems because the supplied directions for use did not contain a recommended service interval.

    Product
    10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1940-2017·2017-05-10

    Anspach Effort Recalls 19cm Pneumatic Attachment Due to Missing Service Interval

    The Anspach Effort, Inc. is recalling 41 units of the 19cm Attachment, Black Max, because the supplied directions for use did not include a recommended service interval.

    Product
    19cm Attachment, Black Max Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1958-2017·2017-05-10

    Anspach Effort 7.2cm Adjustable Drill Guide Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 198 units of the 7.2cm Adjustable Drill Guide because the supplied directions for use did not contain a recommended service interval.

    Product
    7.2cm Adjustable Drill Guide Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2010-2017·2017-05-10

    Anspach Effort Recalls Minimal Access Attachments for Missing Service Interval

    The Anspach Effort, Inc. is recalling 22 Minimal Access Attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    Minimal Access Attachment, BLACK MAX Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1905-2017·2017-05-10

    Breg Inc Recalls Sterile Dressings Due to Potential Unsealed Pouches

    Breg Inc is recalling approximately 2,609 sterile dressings because a small percentage may have unsealed pouches, rendering them non-sterile.

    Product
    Dressing Shldr, P/N 04908 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be applied…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2032-2017·2017-05-10

    Anspach Effort Recalls Heavy Duty Long Heavy Short Attachment

    The Anspach Effort, Inc. is recalling 206 units of the 20.2cm Heavy Duty Long Heavy Short Attachment because the supplied directions for use did not contain a recommended service interval.

    Product
    20.2cm Heavy Duty Long Heavy Short Attachment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1964-2017·2017-05-10

    Anspach Effort Recalls Adjustable Drill Guide for Missing Service Interval

    The Anspach Effort, Inc. is recalling six units of the Adjustable Drill Guide, Black Max because the supplied directions for use did not contain a recommended service interval.

    Product
    ADJUSTABLE DRILL GUIDE, BLACK MAX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1997-2017·2017-05-10

    Anspach Effort Recalls IMRI Short Attachment Pneumatic System Components

    The Anspach Effort, Inc. is recalling 14 IMRI Short Attachment units because the supplied directions for use did not include a recommended service interval.

    Product
    IMRI SHORT ATTACHMENT Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1908-2017·2017-05-10

    Breg Recalls If Hip Sterile Polar Dressings Due to Unsealed Pouches

    Breg Inc is recalling 2,609 units of If Hip Sterile Polar Dressings because some may have unsealed pouches, rendering them non-sterile.

    Product
    If Hip, Sterile Polar Dressing P/N 10680 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1983-2017·2017-05-10

    Anspach Effort Pediatric Craniotome Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling three Pediatric Craniotomes because the supplied directions for use did not contain a recommended service interval.

    Product
    PEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2011-2017·2017-05-10

    Anspach Effort Recalls Minimal Access Straight Driver for Missing Service Interval

    The Anspach Effort, Inc. is recalling 98 Minimal Access Straight Drivers because the supplied directions for use did not contain a recommended service interval.

    Product
    Minimal Access Straight Driver Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2021-2017·2017-05-10

    Anspach Effort Recalls 10.5cm QD Angle Attachment for Pneumatic Systems

    The Anspach Effort, Inc. is recalling 203 units of the 10.5cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.

    Product
    10.5cm QD Angle Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1946-2017·2017-05-10

    Anspach Effort Electronic Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 207 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2001-2017·2017-05-10

    Anspach Pneumatic Attachment Recalled for Missing Service Interval Instructions

    The Anspach Effort, Inc. is recalling 9,829 pneumatic attachments because the supplied directions for use did not include a recommended service interval.

    Product
    12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide