The Recall Desk

State

New Hampshire product recalls

73,817 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,483
Critical
603
Severe
1,049
Most recent
2026-11-04

Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46051–46075 of 78300

  • ModerateFDA (Drugs)·D-0693-2017·2017-05-10

    Amneal Recalls Rabeprazole Sodium Tablets for Failed Dissolution Specifications

    Amneal Pharmaceuticals is recalling Rabeprazole Sodium Delayed Release Tablets, 20 mg, because the product failed to meet dissolution specifications.

    Product
    Rabeprazole Sodium Delayed Release Tablets, 20 mg, a) 30-count bottle (NDC 65162-0724-03), b) 90-count bottle (NDC 65162-0724-09), Rx Only, Manufactured by Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad INDIA 382220, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ 08807
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1915-2017·2017-05-10

    Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Stability Data

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

    Product
    RENOVATION, THIN OSTEOTOME BLADE, 12 MM X 3 INCH, REF 71369212, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2016-2017·2017-05-10

    Anspach Effort Recalls Otologic Curved Micro Pneumatic Systems

    The Anspach Effort, Inc. is recalling 119 Otologic Curved Micro pneumatic systems because the supplied directions for use did not contain a recommended service interval.

    Product
    Otologic Curved Micro Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0689-2017·2017-05-10

    Fluconazole Tablets Recalled for Failed Dissolution Specifications

    The Harvard Drug Group is recalling 914 cartons of Fluconazole 200 mg tablets because they failed to meet required dissolution specifications.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2002-2017·2017-05-10

    Anspach Effort Pneumatic System Attachment Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 247 pneumatic system attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    10.5cm Long Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2019-2017·2017-05-10

    Anspach Effort Oscillating Micro-Saw Pneumatic System Recall

    The Anspach Effort, Inc. is recalling 16 Oscillating MICRO-SAW pneumatic systems because the supplied directions for use did not contain a recommended service interval.

    Product
    Oscillating MICRO-SAW Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1932-2017·2017-05-10

    Anspach Effort AL-III Pneumatic Hose Recall for Missing Service Interval

    The Anspach Effort, Inc. is recalling 17 AL-III pneumatic hose units because the supplied directions for use did not contain a recommended service interval.

    Product
    AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1911-2017·2017-05-10

    Smith & Nephew Recalls Radial Osteotome Blades Due to Shelf Life Data

    Smith & Nephew is recalling 1,126 units of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 14, REF 71369314, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2035-2017·2017-05-10

    Beckman Coulter AQUIOS CL Flow Cytometer Software Export Defect Recall

    Beckman Coulter is recalling AQUIOS CL Flow Cytometers because the software's Export feature incorrectly handles Tetra Combo CRD files.

    Product
    AQUIOS CL Flow Cytometer, Ref no. B30166, Software Versions 2.0 and 2.0.1 Product Usage: The AQUIOS CL Flow Cytometer is intended for use with in vitro diagnostic flow cytometric applications using up to four fluorescent detection channels using a blue (488 nm) laser, two…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1907-2017·2017-05-10

    Breg Inc Recalls Dressing Back P/N 09810 Due to Unsealed Pouches

    Breg Inc is recalling 2,609 units of Dressing Back P/N 09810 because approximately 0.22% may have unsealed pouches, rendering them non-sterile.

    Product
    Dressing Back, P/N 09810 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-2017-2017·2017-05-10

    Anspach Effort 45 Degree Contra Angle Attachment Recall for Missing Service Interval

    The Anspach Effort, Inc. is recalling 45 degree Contra Angle Attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    45 degree Contra Angle Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2013-2017·2017-05-10

    Anspach Effort Pneumatic Attachment Recalled for Missing Service Interval Instructions

    The Anspach Effort, Inc. is recalling 8.0CM Heavy Duty Medium Pneumatic Attachments because the supplied directions for use did not contain a recommended service interval.

    Product
    8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1948-2017·2017-05-10

    Anspach Electronic Foot Control Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 209 Electronic Foot Controls with Direction Switches because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction Switch Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2027-2017·2017-05-10

    Anspach Effort Recalls Jacobs Chuck Attachment Due to Missing Service Interval

    The Anspach Effort, Inc. is recalling 50 units of the SMALL ATTACHMENT, JACOBS CHUCK because the supplied directions for use did not contain a recommended service interval.

    Product
    SMALL ATTACHMENT, JACOBS CHUCK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1919-2017·2017-05-10

    Smith & Nephew Recalls Osteotome Blades Due to Shelf Life Data

    Smith & Nephew is recalling 1,741 units of Renovation osteotome blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, ROUNDED END, THIN OSTEOTOME BLADE, 12 MM, REF 71369412, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2004-2017·2017-05-10

    Anspach Effort Bearing Sleeve Recall for Missing Service Interval

    The Anspach Effort, Inc. is recalling 112 Bearing Sleeves because the supplied directions for use did not contain a recommended service interval.

    Product
    Bearing Sleeve, 10CM Straight Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide