State

New Hampshire product recalls

73,737 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,482
Critical: 603
Severe: 1,048
Most recent: 2026-10-28

Of the 4,482 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 1,048 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30851–30875 of 78219

ModerateFDA (Devices)·Z-1608-2020·2020-04-08
Trilliant Surgical Disco Subtalar Implant Instructions for Use Recall
Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for the Disco Subtalar Implant System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Disco Subtalar Implant System, Model 112-00-001. The firm name on the label is Trilliant Surgical, Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1630-2020·2020-04-08
Natus Olympic Brainz Monitor Recalled for Missing Functional Tests
Natus Neurology is recalling 40 Olympic Brainz Monitors because required functional tests were not performed before release, meaning the manufacturer cannot verify system functionality.
Product
natus newborn care Olympic Brainz Monitor, REF OBM00002. electroencephalograph
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1614-2020·2020-04-08
Trilliant Surgical Small Joint Reaming System Instructions for Use Recall
Trilliant Surgical LLC is recalling Instructions for Use and Cleaning Protocols for the Small Joint Reaming System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Small Joint Reaming System, Model 311-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1627-2020·2020-04-08
Conformis Recalls iTotal CR Knee Replacement System Due to Labeling Error
Conformis, Inc. is recalling four iTotal CR Knee Replacement System kits because they were labeled with incorrect serial numbers and delivered to the wrong customers.
Product
iTotal CR Knee Replacement System, Model No. TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT) - Product Usage: The iTotal CR Knee Replacement System is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1623-2020·2020-04-08
Gentell Hydrogel Ag Gauze Recalled for FDA Registration Failure
Gentell, Inc. is recalling 53,134 units of Gentell Hydrogel Ag 2x2 gauze because the product was not properly registered with the FDA.
Product
Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1607-2020·2020-04-08
Trilliant Surgical Twist Sublatar Implant System Instructions for Use Recall
Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for the Twist Sublatar Implant System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning Sterilization Protocol for Trilliant Surgical Ltd Twist Sublatar Implant System, Model 112-00-001. The firm name on the label is Trilliant Surgical, Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1613-2020·2020-04-08
Trilliant Surgical Gridlock Ankle Plating System Instructions for Use Recalled
Trilliant Surgical LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for the Gridlock Ankle Plating System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Ankle Plating System, Model 320-01-100. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1610-2020·2020-04-08
Trilliant Surgical Recalls Hammertoe Implant Instructions for Use
Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for its Two-Step Hammertoe Implant System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Two-Step Hammertoe Implant System, Model 214-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1617-2020·2020-04-08
Haemonetics Recalls TEG Manager Software Due to Alert Display Defect
Haemonetics is recalling TEG Manager software versions 1.1.0 through 4.1.1 because a defect causes incorrect out-of-range alerts for coagulation test results.
Product
TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0, 3.0.0, 4.0.0, 4.1.0 and 4.1.1. Intended: For in vitro coagulation studies
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1601-2020·2020-04-08
Butterfly iQ Ultrasound System Recalled for Lack of FDA Approval
Butterfly Network, Inc. is recalling 11,183 Butterfly iQ Ultrasound Systems because they were distributed without an approved 510(k).
Product
Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction) Tool REF/Model: 850-20003 UDI: (01)00866646000206 Software versions 1.10.0, 1.11.0, 1.12.0, 1.13.0, 1.13.0, 1.14.0, 1.15.0 Product Usage: Intended use: Diagnostic ultrasound imaging and measurement of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2020·2020-04-08
Trilliant Surgical 3S Hemi Toe Implant Instructions for Use Recall
Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for the 3S Hemi Toe Implant System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd 3S Hemi Toe Implant System, Model 111-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1606-2020·2020-04-08
Trilliant Surgical Recalls Instructions for Use for Tiger Screw Systems
Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for Tiger Screw Systems to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Headless Cannulated Screw System, Model 212-00-001; and (2) Combination Tiger Cannulated/Tiger Headless Cannulated Screw System, Model 210-00-101. The firm name…
Category
Medical Device
Distribution
29 states
ModerateFDA (Drugs)·D-1079-2020·2020-04-08
Lupin Recalls Lisinopril Tablets Due to Foreign Tablet Mix-Up
Lupin Pharmaceuticals is recalling 25,944 bottles of Lisinopril 30 mg tablets because a 5 mg tablet was found mixed into a 30 mg bottle.
Product
LISINOPRIL — LISINOPRIL (LISINOPRIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1628-2020·2020-04-08
Conformis Recalls iTotal PS Knee Replacement System Due to Labeling Error
Conformis is recalling two iTotal PS Knee Replacement System kits because tibial trays were labeled with incorrect serial numbers and delivered to the wrong customers.
Product
iTotal PS Knee Replacement System, Model No. TPS-111-1111-010101, (ITOTAL PS IPOLY IMPLANT KIT LEFT) Product Usage: The iTotal CR Knee Replacement System is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1609-2020·2020-04-08
Trilliant Surgical Gridlock Plating System Instructions for Use Recall
Trilliant Surgical is recalling Instructions for Use and Cleaning Protocols for the Gridlock Plating System to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Plating System, Model 310-01-100. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1624-2020·2020-04-08
Gentell Hydrogel Ag Gauze Recalled for FDA Registration Deficiency
Gentell, Inc. is recalling 20,025 units of Gentell Hydrogel Ag 4x4 gauze because the product was not properly registered with the FDA.
Product
Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1600-2020·2020-04-08
Butterfly iQ Ultrasound System Auto Bladder Volume Tool Recalled for Regulatory Violation
Butterfly Network, Inc. is recalling the Butterfly iQ Ultrasound System Auto Bladder Volume Tool because it was distributed without an approved 510(k).
Product
Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentation measurement tool REF/Model: 850-20003 Software versions 1.13.0, 1.14.0, and 1.15.0 - Product Usage: Butterfly iQ is indicated for use by qualified and trained healthcare…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1612-2020·2020-04-08
Trilliant Surgical Recalls Instructions for Use for Cannulated Screw Systems
Trilliant Surgical, LLC is recalling Instructions for Use and Surgical Cleaning and Sterilization Protocols for two cannulated screw systems to update dry time parameters.
Product
Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Large Cannulated Screw System, Model 215-00-001; and (2) Trilliant Surgical Ltd Large Cannulated Headless Screw System, Model 215-00-001. The firm name on the…
Category
Medical Device
Distribution
29 states
LowFDA (Drugs)·D-1258-2020·2020-04-08
Akorn Recalls Fentanyl Citrate Injection Due to Impurity Specification Failure
Akorn Inc. is recalling Fentanyl Citrate Injection, USP, 100 mcg/2 mL, because retained sample testing showed total impurities exceeded the allowed limit.
Product
Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 10 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-02
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1625-2020·2020-04-08
Gentell Hydrogel Ag Saturated Gauze Recalled for FDA Registration Deficiency
Gentell, Inc. is recalling 6,433 units of Gentell Hydrogel Ag Saturated Gauze because the product was not properly registered with the FDA.
Product
Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1626-2020·2020-04-08
Gentell Hydrogel Ag Wound Dressing Recalled for Registration Issues
Gentell, Inc. is recalling Gentell Hydrogel Ag wound dressings because the product was not properly registered with the FDA.
Product
Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Silver Antimicrobial Wound Dressing is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V200000·2020-04-07
Terex Recalls 2018-2019 Digger Derrick Vehicles Due to Engine Software Error
Terex is recalling 2018-2019 Digger Derrick vehicles because an engine computer error can disable remote engine stop functions, increasing injury risk during hydraulic issues.
Product
TEREX — TEREX DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V201000·2020-04-07
Vac-Tron Recalls Vacuum Excavator Trailers for Lighting Defects
Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper lighting and missing reflectors may reduce visibility at night, increasing crash risk.
Product
VAC-TRON — VAC-TRON MC 535, MC 533 SDT, MINICOMBO, MC 573 SDT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V204000·2020-04-07
Vac-Tron Recalls 2012-2020 Vacuum Excavator Trailers for Lighting Defects
Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper exterior lighting and missing reflectors may reduce visibility at night, increasing crash risk.
Product
VAC-TRON — VAC-TRON MC 873 SDT, MC 855 SDT, MC 833 SDT, MC 835 SDT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V198000·2020-04-06
KTM Recalls 2019-2020 790 Adventure Models Due to Rear Brake Hose Overheating
KTM is recalling 2019-2020 790 Adventure and 790 Adventure R motorcycles because the rear brake hose may overheat, potentially causing brake failure and increasing crash risk.
Product
KTM — KTM 790 ADVENTURE R, 790 ADVENTURE
Category
Vehicle
Distribution
Distributed nationwide