State

New Hampshire product recalls

73,576 recalls have nationwide distribution and so reach New Hampshire. 4,477 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,477
Critical: 606
Severe: 1,045
Most recent: 2026-10-21

Of the 4,477 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,045 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,477 recalls whose distribution notice names New Hampshire specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26476–26500 of 78053

SevereFDA (Devices)·Z-1306-2021·2021-04-07
Medtronic Recalls CRT-D Devices Due to Shortened Replacement Time
Medtronic is recalling specific CRT-D implantable cardioverter defibrillators because a small percentage may experience a shortened time before the device reaches end of service.
Product
Implantable cardioverter defibrillators (ICD) with cardiac resynchronization therapy (CRT-D): 1) Viva family: Viva XT CRT-D, Viva XT Quad CRT-D, Viva S CRT-D, Viva Quad S CRT-D and Viva Quad C CRT-D models; 2) Claria family: Claria MRI CRT-D and Claria MRI Quad CRT-D models; 3)…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1309-2021·2021-04-07
CareFusion Recalls BD Alaris Infusion Pump Keypads Due to Fluid Ingress
CareFusion is recalling BD Alaris Infusion Pump Module Keypads and Door Assembly Kits because fluid ingress can cause unresponsive or stuck keys, potentially delaying medication infusion.
Product
BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad; and Pump Module Door Assembly Replacement Kit with Pump Module Keypad, Parts: 49000239; 49000346; 49000438; 49000439.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0315-2021·2021-04-07
Zydus Recalls Acyclovir Sodium Injection Due to Crystallization
Zydus Pharmaceuticals is recalling Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
Product
ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V244000·2021-04-07
New Flyer Recalls Electric Buses Due to Inverter Firmware Errors
New Flyer is recalling certain 2013-2021 electric buses because firmware errors in the inverters may cause the electric drive system to shut down, increasing the risk of a crash.
Product
NEW FLYER — NEW FLYER XE60, XE35, XE40, XHE40
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1313-2021·2021-04-07
Medtronic Bio-Console 560 Blood Pumping Console Recalled for Electrical Failure
Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.
Product
Medtronic Bio-Console 560 Extracorporeal Blood Pumping Console, Model Numbers: 560BC, 560BC1, 560BCS, 560BCS1, R560BCS1. Used in cardiopulmonary bypass (CPB) procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V243000·2021-04-07
Utility Trailer Recalls VS2DC, VS2DX, VS3DX Models for Missing Weld
Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.
Product
UTILITY TRAILER — UTILITY TRAILER VS3DX, VS2DX, VS2DC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1330-2021·2021-04-07
Siemens ACUSON Sequoia Ultrasound Systems Recalled for Incorrect Delivery Date Calculations
Siemens is recalling 1,172 ACUSON Sequoia ultrasound systems because a software error may calculate incorrect Estimated Dates of Delivery, potentially influencing clinical decisions.
Product
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-1323-2021·2021-04-07
Nuvasive PRECICE STRYDE Intramedullary Nail Recall for Biological Safety Concerns
Nuvasive Specialized Orthopedics is recalling PRECICE STRYDE intramedullary nails due to complaints of adverse events potentially related to biological safety, including pain and bony abnormalities.
Product
PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21103·2021-04-07
Epicure Recalls Glass Prep Bowls Due to Laceration Hazard
Epicure is recalling glass prep bowls that may shatter during use, posing a laceration hazard. Consumers should stop using the product and contact Epicure for a free replacement.
Product
Epicure Prep Bowls (Set of Four)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0317-2021·2021-04-07
Ferring Recalls ZOMA-Jet 5 Demonstration Kits Due to Defective Delivery System
Ferring Pharmaceuticals is recalling 301 ZOMA-Jet 5 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.
Product
ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 5mg vial, Rx only, ZOMA-Jet 5 Demonstration Kit contains -ZOMA-Jet 5 device - 5 Needle-Free Head A's - 2 Vial Adaptors - 1 Carrying Case - 1 User Manual; Manufactured for…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21102·2021-04-07
RH Recalls Children's Bath Wraps for Flammability Standard Violations
RH is recalling approximately 55,700 children's bath wraps in the U.S. because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Product
Animal, Heathered Plush and Luxe Sherpa Children's Bath Wraps
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1324-2021·2021-04-07
Nuvasive Precice Bone Transport Nail Recalled for Biological Safety Concerns
Nuvasive Specialized Orthopedics is recalling 226 Precice Bone Transport nails due to complaints of pain and bony abnormalities related to biological safety.
Product
Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1328-2021·2021-04-07
Alcon Custom Ophthalmic Surgical Procedure Packs Recalled for Mold
Alcon is recalling 249,853 custom ophthalmic surgical procedure packs because mold was found on gowns included in the packages.
Product
Alcon Custom Ophthalmic Surgical Procedure Packs
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1342-2021·2021-04-07
Diasorin Recalls LIAISON 1-84 PTH Assay Due to Falsely Elevated Results
Diasorin Inc. is recalling LIAISON 1-84 PTH Assay kits because the system may produce falsely elevated parathyroid hormone results.
Product
LIAISON 1-84 PTH Assay - Product Usage: is an in vitro chemiluminescent immunoassay (CLIA) intended for the quantitative determination of parathyroid hormone (1-84) in human serum and EDTA plasma. Measurements of parathyroid hormone levels are used in the differential diagnosis…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1325-2021·2021-04-07
Nuvasive Recalls PRECICE Plates Due to Biological Safety Concerns
Nuvasive Specialized Orthopedics Inc is recalling 40 PRECICE Plate units worldwide due to complaints of adverse events potentially related to biological safety.
Product
PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1311-2021·2021-04-07
Hollister Recalls Vertical Drain Tube Attachment Devices Due to Separation Risk
Hollister Incorporated is recalling Vertical Drain Tube Attachment Devices (VTAD) because the tube holder can separate from the securing barrier, risking tube migration or loss.
Product
Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0318-2021·2021-04-07
Ferring Recalls ZOMA-Jet 10 Demonstration Kits Due to Defective Delivery System
Ferring Pharmaceuticals is recalling 1,569 ZOMA-Jet 10 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.
Product
ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial, ZOMA-Jet 10 Demonstration Kit contains -ZOMA-Jet 10 device - 7 Needle-Free Head A's - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1315-2021·2021-04-07
DePuy Orthopaedics Recalls Mobile Bearing Total Knee Systems Due to Packaging Damage
DePuy Orthopaedics is recalling specific lots of the LCS COMPLETE P.F.C. SIGMA RP Mobile Bearing Total Knee System because of potential damaged packaging.
Product
The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee System - Product Usage: consists of three components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1329-2021·2021-04-07
Oscor SafeSheath ULTRALITE 10F Recalled for Potential Open Sterile Seal
Oscor, Inc. is recalling 500 units of the AngioDynamics SafeSheath ULTRALITE 10F due to a potential open seal on the sterile product.
Product
AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various types of pacing leads and catheters.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1327-2021·2021-04-07
Stryker Harmonic ACE +7 Shears Recalled for Lack of Regulatory Clearance
Stryker is recalling 102 units of Harmonic ACE +7 Shears because they were distributed without receiving regulatory clearance.
Product
Stryker Sustainability Solutions REF HARH36 Ethicon Endo-Surgery, Inc. Harmonic ACE +7, Shears with Advanced Hemostasis 5mm Diameter x 36cm - Product Usage: indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. The instruments can be…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1312-2021·2021-04-07
LumiraDx Coronavirus Antigen Test Strips Recalled for False Positives
LumiraDx is recalling 2,186 coronavirus antigen test strips because two lots failed quality control testing and produced false positives.
Product
Coronavirus antigen detection test system - Product Usage: intended for the qualitative detection of the nucleocapsid protein antigen to SARS-CoV-2 directly from nasal swab samples collected from individuals suspected of COVID-19 by their healthcare provider within the first…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1316-2021·2021-04-07
DePuy ATTUNE Rotating Platform Total Knee System Recalled for Damaged Packaging
DePuy Orthopaedics is recalling 355 units of the ATTUNE Rotating Platform Total Knee System due to potential damaged packaging. The affected tibial bases are used in cemented total knee arthroplasty.
Product
The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Usage: consists of multiple components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1314-2021·2021-04-07
DePuy ATTUNE Knee Implant Recall for Damaged Packaging
DePuy Orthopaedics is recalling ATTUNE and MBT tibial base components used in knee replacements due to potential damaged packaging.
Product
ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components designed to replace the natural articular surface of the knee joint. The femoral component is a metal implant without a porous coating. The tibial component may…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1310-2021·2021-04-07
Arthrex Recalls Cannulated Drill Bits Due to Incorrect Color Indicator
Arthrex, Inc. is recalling 9 units of 5.0 mm cannulated drill bits because the color indicator on the shaft is the incorrect color.
Product
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V241000·2021-04-06
Mercedes-Benz and Freightliner Sprinter Recalled for Steering Hose Defect
Daimler Vans USA is recalling 2019-2020 Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER (VS30), SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide