State

New Hampshire product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37901–37925 of 78289

HighFDA (Devices)·Z-0461-2019·2018-11-21
Medtronic Recalls Parietex Composite Parastomal Mesh Due to Failure Reports
Medtronic is voluntarily removing Parietex Composite Parastomal Mesh from the market after receiving reports of product failure leading to hernia recurrence.
Product
Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20) Product Usage: The PCOPM15 and PCOPM20 reorder codes are circular in shape, made from a three-dimensional monofilament polyester fabric with a two-dimensional monofilament polyester central band. One side…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0420-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold 20x20cm devices because the suture material degraded, causing them to fail burst specifications after 18 months.
Product
OviTex Reinforced BioScaffold 20x20cm, Part Number F10254-2020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0454-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 130 Deg 12x165mm, Item Number 816812165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold 10x12cm devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0433-2019·2018-11-21
AROA Biosurgery Recalls OviTex 2S Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex 2S Reinforced BioScaffold devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex 2S Reinforced BioScaffold 20x20cm, Part Number F10258-2020G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0412-2019·2018-11-21
GE Healthcare Recalls Aisys Anesthesia Systems Due to Ventilation Mode Defect
GE Healthcare is recalling Aisys anesthesia systems because they may fail to transition to backup ventilation if a patient stops breathing spontaneously.
Product
Aisys CS2 Anesthesia System. Sold under the following product names: AISYS, AISYS 10.X TO 11.X UPGRADE KIT DUTCH, AISYS 10.X TO 11.X UPGRADE KIT ENGLISH, AISYS 10.X TO 11.X UPGRADE KIT ENGLISH FOR USA, AISYS 10.X TO 11.X UPGRADE KIT FRENCH, AISYS 10.X TO 11.X UPGRADE KIT…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0415-2019·2018-11-21
AROA Biosurgery Recalls OviTex Reinforced BioScaffold Mesh Devices
AROA Biosurgery is recalling OviTex Reinforced BioScaffold 4x8cm devices because the suture material degraded, causing them to fail burst specifications.
Product
OviTex Reinforced BioScaffold 4x8cm, Part Number F10254-0408G
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0439-2019·2018-11-21
Stryker Spirit Select Bed Recall for Potential Entrapment Risk
Stryker is recalling Spirit Select Beds with high rail siderails due to non-compliance with safety standards and a potential risk of entrapment.
Product
The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option
Category
Medical Device
Distribution
50 states
ModerateFDA (Devices)·Z-0457-2019·2018-11-21
Siemens Artis zee Biplane Systems Recalled for C-Arm Vibration Issues
Siemens is recalling 14 Artis zee biplane systems because C-arm vibrations may reduce image quality due to a ceiling support screw connection.
Product
ARTIS zee biplane systems with Material 10094141- a Angiographic x-ray system Product Usage: Artis zee is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0278-2019·2018-11-21
Taro Recalls Children's Allergy Relief Oral Solution Due to Impurity
Taro Pharmaceuticals is recalling specific bottles of children's allergy relief oral solution because an unknown impurity exceeded safety limits during routine testing.
Product
children's allergy relief (cetirizine hydrochloride) oral solution, 1 mg/mL, Dye Free, Sugar Free, Alcohol Free, 4 FL OZ (120 mL) bottle, Distributed by Rite-Aid, 30 Hunter Lane, Camp Hill, PA 17011, Made in Israel, UPC 0 11822 57363 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0464-2019·2018-11-21
Abbott TECNIS Intraocular Lenses Recalled for Expiration Date Violations
Johnson & Johnson Surgical Vision is recalling 17 expired Abbott TECNIS intraocular lenses distributed in seven US states.
Product
Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Preloaded Delivery System, Lens Model PCB00, Sterile, Rx - Product Usage: The lenses are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0465-2019·2018-11-21
Siemens Lipase Reagent Cartridge Recall for Lot Variability
Siemens Healthcare is recalling specific lots of Dimension Lipase Flex Reagent Cartridges due to lot-to-lot variability affecting quality control and patient results.
Product
Dimension Lipase Flex Reagent Cartridge, Model Number 10460277 Product Usage: Dimension - The LIPL method is an in vitro diagnostic test for the quantitative measurement of lipase in human serum and plasma on the Dimension¿ clinical chemistry system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0466-2019·2018-11-21
Siemens Dimension Vista Lipase Reagent Cartridge Recalled for Variability
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista Lipase Flex Reagent Cartridges due to lot-to-lot variability in quality control and patient results.
Product
Dimension Vista Lipase Flex Reagent Cartridge, Model Number 10461745 Product Usage: Dimension Vista - The LIPL method is an in vitro diagnostic test for the quantitative measurement of lipase in human serum and plasma on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0468-2019·2018-11-21
Arrow Multi-Lumen CVC Kit Recalled for Labeling Inconsistencies
Arrow International is recalling 3,640 units of the AGB+ Multi-Lumen CVC Kit because some labels incorrectly state the spring-wire guide size as .032 instead of .025.
Product
Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code CDC-45703-B1A - Product Usage: The multiple-lumen catheter permits venous access to the central circulation by the way of the femoral, jugular, or subclavian…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0459-2019·2018-11-21
Siemens Artis Q.zen Biplane X-Ray System Recalled for C-Arm Vibration
Siemens Medical Solutions is recalling 15 Artis Q.zen biplane angiographic x-ray systems because C-arm vibrations may reduce image quality.
Product
ARTIS Q.zen biplane with Material 10848355 - a Angiographic x-ray system Product Usage: Artis zee is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0444-2019·2018-11-21
Espiner Tissue Retrieval System Recalled for Incorrect Volume Labeling
Espiner Medical Ltd is recalling 230 units of the Eco-Sac Tissue Retrieval System because the label incorrectly states the volume is 1200 ml instead of 1000 ml.
Product
Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage: Tissue Retrieval sac made from ripstop nylon. The EMP160ECO-US-5 is a semi-automatic sac, which incorporates a monofilament drawstring around the mouth of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0455-2019·2018-11-21
Straumann Recalls Neodent GM Mini Conical Abutments Due to Label Mismatch
Straumann Manufacturing is recalling 21 units of Neodent GM Mini Conical Abutments because the laser-engraved label does not match the item in the package.
Product
Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Abutments are intermediary prosthetic components to be installed onto GM implants to support the final prosthesis. They are provided in a rotational shape for the coupling with the prosthesis and in different…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0446-2019·2018-11-21
BioFire FilmArray Meningitis/Encephalitis Panel Recalled for False Positive Risk
BioFire Diagnostics is recalling specific FilmArray Meningitis/Encephalitis (ME) Panel kits due to a manufacturing issue that may cause elevated rates of false positive results for HSV-1.
Product
-Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME) Panel REF RFIT-ASY-0118 30 For FilmArray systems LOT KIT UDI (01)00815381020123 CE 0086 IVD -Fitment Label (P/N RFIT-LBL-0138) which identifies the pouch label - FilmArray¿ ME Panel v1.4…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0277-2019·2018-11-21
Taro Recalls Children's Allergy Oral Solution Due to Impurity
Taro Pharmaceuticals is recalling 8,328 bottles of Children's Allergy (cetirizine hydrochloride) oral solution because an unknown impurity exceeded specified limits during stability testing.
Product
CHILDRENS ALLERGY — CHILDRENS ALLERGY (CETIRIZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0458-2019·2018-11-21
Siemens ARTIS Q Biplane Recalled for C-Arm Vibration Issues
Siemens is recalling 54 ARTIS Q biplane x-ray systems because C-arm vibrations may reduce image quality due to a ceiling support screw connection.
Product
ARTIS Q biplane with Material 10848282- - a Angiographic x-ray system Product Usage: Artis zee is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0257-2019·2018-11-21
Sandoz Recalls Nitrofurantoin Capsules Due to Cross Contamination
Sandoz Inc is recalling specific lots of Nitrofurantoin capsules because they may be cross-contaminated with other products.
Product
NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS) — NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS) (NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS))
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0279-2019·2018-11-21
Breckenridge Recalls Megestrol Acetate Oral Suspension for Stability Failures
Breckenridge Pharmaceutical is recalling Megestrol Acetate Oral Suspension due to out-of-specification particle size results during stability testing.
Product
Megestrol Acetate Oral Suspension, USP 625 mg/5mL, 150 mL bottle, Rx only, Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487, Manufactured by: Pharmaceutics International Inc. Hunt Valley, MD 21031
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0262-2019·2018-11-21
Sandoz Recalls Nitrofurantoin Capsules Due to Cross-Contamination
Sandoz Inc. is recalling specific lots of Nitrofurantoin Capsules 100 mg due to cross-contamination with other products.
Product
Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, 100-count bottoles, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141 Manufactured by: Sandoz Inc. Princeton, NJ 08540,NDC 16714-439-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V823000·2018-11-20
Grand Design Recalls 2019 Imagine Trailers Due to Bearing Defect
Grand Design is recalling 2019 Imagine recreational trailers because inner hub bearings may overheat and fail, increasing crash risk.
Product
GRAND DESIGN — GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·116-2018·2018-11-20
Long Phung Recalls Pork Products Due to Possible Listeria Contamination
Long Phung Food Products is recalling ready-to-eat pork products due to possible Listeria monocytogenes contamination linked to four confirmed illnesses.
Product
165368 C. Corporation — 165368 C. Corporation Recalls Pork Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide