State

New Hampshire product recalls

73,596 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: 603
Severe: 1,048
Most recent: 2026-10-21

Of the 4,477 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 4,477 recalls whose distribution notice names New Hampshire specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28201–28225 of 78073

SevereFDA (Devices)·Z-0255-2021·2020-10-28
ICU Medical Recalls Intravascular Administration Sets Due to Manufacturing Defect
ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect on the NanoClave may prevent a proper seal with the spike.
Product
148 IN (376cm) APPX 18.8 ml, 15 DROP SET, 2 CLAVE, Remv 3 Gang Clave Stopcock.1 unit per pouch, 25 pouches per case. UDI:(01)10887709071558(17)250101(30)25(10)4603841. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0222-2021·2020-10-28
ICU Medical Recalls Intravascular Administration Sets Due to Seal Defect
ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent a proper seal.
Product
123 IN (312cm) APPX 16.1 ml, 10 DROP SET w/3 MicroClave, 3-Port NanoClave; UDI:(01)10887709085432(17)241201(30)25(10)4536733;(01)10887709085432(17)250101(30)25(10)4573641. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0130-2021·2020-10-28
GE Healthcare Recalls MRI Systems Due to Electrical Arc Flash Risk
GE Healthcare is recalling 30 MRI systems worldwide due to a potential electrical arc flash hazard within the Power Gradient & RF Cabinet.
Product
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0059-2021·2020-10-28
Sauer Brands Recalls The Spice Hunter Cilantro Jars Due to Salmonella Risk
Sauer Brands Inc is recalling The Spice Hunter Cilantro jars due to potential Salmonella contamination. The product was distributed nationwide and online.
Product
The Spice Hunter Cilantro 0.3 oz. Jar UPC 8105701236 Case UPC 40081057012367
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0040-2021·2020-10-28
Sauer Brands Recalls Saigon Organic Cinnamon Jars Due to Salmonella Risk
Sauer Brands Inc is recalling Saigon Organic Cinnamon jars due to potential Salmonella contamination. The product was sold nationwide and online.
Product
The Spice Hunter Saigon Organic Cinnamon 1.7 oz. Jar UPC 8105701245 Case UPC 40081057012459
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0048-2021·2020-10-28
Sauer Brands Recalls Green Hatch Chile Jars Due to Salmonella Risk
Sauer Brands Inc is recalling specific jars of The Spice Hunter Green Hatch Chile due to potential Salmonella contamination. Consumers should check their pantries for the affected lot.
Product
The Spice Hunter Green Hatch Chile 2.4 oz. Jar UPC 8105702256 Case UPC 40081057022564
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0042-2021·2020-10-28
Sauer Brands Recalls Sesame Seeds Due to Potential Salmonella Contamination
Sauer Brands Inc is recalling The Spice Hunter Gourmet Sesame Seeds due to potential Salmonella contamination. The product was distributed nationwide and online.
Product
The Spice Hunter Gourmet Sesame Seeds 2.4 oz. Jar UPC 8105701937 Case UPC 40081057019373
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0055-2021·2020-10-28
Sauer Brands Recalls Everything Bagel Crunch for Potential Salmonella
Sauer Brands Inc is recalling The Spice Hunter Everything Bagel Crunch due to potential Salmonella contamination. The product was distributed nationwide and online.
Product
The Spice Hunter Everything Bagel Crunch 2.3 oz. Jar UPC 8105701351 Case UPC 40081057013517
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0111-2021·2020-10-28
Vascular Solutions Recalls Langston Dual Lumen Catheters Due to Lumen Separation
Vascular Solutions, Inc. is recalling 89,121 Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.
Product
Langston Dual Lumen Catheter.
Category
Medical Device
Distribution
52 states
SevereFDA (Food)·F-0049-2021·2020-10-28
Sauer Brands Recalls Black Pepper Jars Due to Salmonella Risk
Sauer Brands Inc is recalling specific jars of The Spice Hunter Black Pepper and Fine Black Pepper due to potential Salmonella contamination.
Product
The Spice Hunter Black Pepper 1.7 oz. Jar UPC 8105701703 Case UPC 40081057017034, Fine Black Pepper 1.6 oz. Jar UPC 8105701706 Case UPC 40081057017065
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0258-2021·2020-10-28
ICU Medical Recalls Burette Sets Due to Potential Manufacturing Defect
ICU Medical is recalling specific lots of 112-inch burette sets because a manufacturing defect may prevent a proper seal with the NanoClave spike.
Product
112" (284 cm) 60 Drop 150ml Burette Set (Clave, Shut-Off) w/2 MicroClave, Remv 3 Gang 4-Way Clave Stopcock, Check Valve, Rotating Luer, 1 Ext. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709079127(17)250201(30)25(10)4727501. The Intravascular Administration Set is a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0176-2021·2020-10-28
Bien-Air Surgery Foot Pedal Recalled Due to Magnet Detachment Risk
Bien-Air Surgery is recalling 1,120 foot pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.
Product
Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODOC - Product Usage: intended to convert electrical energy to mechanically drive handpieces and microsaws used to cut and shape bones.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0036-2021·2020-10-28
Acella Recalls NP Thyroid 15 Tablets Due to Subpotent Levothyroxine Levels
Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because FDA analysis found the levothyroxine content was less than labeled.
Product
NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0203-2021·2020-10-28
ICU Medical Recalls Smallbore Intravascular Administration Sets Due to Seal Defect
ICU Medical is recalling specific lots of smallbore intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Product
8.5" (22 cm) Appx 0.57 ml, Smallbore Ext Set w/NanoClave, 0.2 Micron Filter, Clamp, Rotating Luer;1 unit per pouch, 50 multivac pouches per case.UDI:(01)10887709077671(17)250101(30)50(10)4557524. The Intravascular Administration Set is a single use, sterile, non-pyrogenic…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0043-2021·2020-10-28
Sauer Brands Recalls Herbs De Provence Jars Due to Salmonella Risk
Sauer Brands Inc is recalling specific lots of The Spice Hunter Herbs De Provence due to potential Salmonella contamination.
Product
The Spice Hunter Herbs De Provence 0.6 oz. Jar UPC 8105701440 Case UPC 40081057014408
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0112-2021·2020-10-28
Vascular Solutions Recalls Langston Dual Lumen Catheters Due to Separation Risk
Vascular Solutions, Inc. is recalling 1,745 Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.
Product
Langston Dual Lumen Catheter.
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0221-2021·2020-10-28
ICU Medical Recalls NanoClave Intravascular Administration Sets Due to Seal Defect
ICU Medical is recalling specific lots of NanoClave intravascular administration sets because a manufacturing defect may prevent a proper seal with the spike.
Product
83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way NanoClave¿ Stopcock w/Baseplate, Rotating Luer;1 unit per pouch, 25 pouches per case. UDI:(01)10887709089508(17)250101(30)25(10)4548244. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0186-2021·2020-10-28
ICU Medical Recalls Smallbore Extension Sets Due to Seal Defect
ICU Medical is recalling specific lots of 7-inch smallbore extension sets because a manufacturing defect may prevent the NanoClave from sealing properly.
Product
7" (18 cm) Appx 0.29 ml, Smallbore Ext Set w/MicroClave Clear, NanoClave, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709051048(17)250101(30)50(10)4572718; (01)10887709051048(17)250101(30)50(10)4603246…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2021·2020-10-28
ICU Medical Recalls Intravascular Administration Sets Due to Manufacturing Defect
ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Product
40 (102cm) Appx 4.4ml Ext Set, 4-Way Clave Stopcock, Clave, 2 Clamps, Rotating Luer, 1 Ext. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709014531(17)250101(30)50(10)4603496. The Intravascular Administration Set is a single use, sterile, non-pyrogenic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0193-2021·2020-10-28
ICU Medical Recalls Smallbore Pressure Infusion Extension Sets
ICU Medical is recalling specific lots of smallbore pressure infusion extension sets due to a potential manufacturing defect that may inhibit a proper seal.
Product
6.5" (17 cm) Appx 0.30 ml, Smallbore Pressure Infusion (400psig) Ext Set w/Remv MicroClave, NanoClave T-Connector, Purple Clamp, Rotating Luer. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709062525(17)250101(30)50(10)4558455…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0182-2021·2020-10-28
ICU Medical Recalls NanoClave Connectors Due to Manufacturing Defect
ICU Medical is recalling specific lots of NanoClave Connectors because a manufacturing defect may prevent a proper seal with the spike.
Product
NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051; (01)10887709051017(17)241101(30)100(10)4447754 CLAVE Neutron is a normally closed, bidirectional connector intended for use as an accessory to an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0172-2021·2020-10-28
Smith & Nephew Recalls HEALICOIL Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling HEALICOIL absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK- Absorbable Suture anchor Product Number: 72203708
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0259-2021·2020-10-28
ICU Medical Recalls Smallbore Trifuse Extension Sets Due to Seal Defect
ICU Medical is recalling specific lots of Smallbore Trifuse Extension Sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Product
5.5" (14 cm) Appx 0.39 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, NanoClave T-Connector, 3 Clamps, Rotating Luer.1 unit per pouch, 50 multivac pouches per case. UDI: (01)10887709032153(17)241101(30)50(10)4475297; (01)10887709032153(17)250201(30)50(10)4711598. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0153-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.9 W. 2 UB WHITE / BLACK -Absorbable Suture anchor Product Number: 72201996
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0267-2021·2020-10-28
ICU Medical Recalls NanoClave Administration Sets Due to Seal Defect
ICU Medical is recalling specific lots of NanoClave administration sets because a manufacturing defect may prevent the NanoClave from sealing properly.
Product
135 cm (53") Ext Set w/Remv 5 Gang Stopcock, Baseplate w/7 NanoClave, 4-Way Stopcock, Rotating Luer, 1 Ext..1 unit per pouch, 25 pouches per case. UDI:(01)10840619060616(17)250201(30)25(10)4711366. Administration sets and their accessories are single use, pre-sterilized…
Category
Medical Device
Distribution
Distributed nationwide