State

New Hampshire product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34551–34575 of 78223

ModerateFDA (Drugs)·D-1494-2019·2019-07-31
Pharma-Natural Recalls Army Health Pain Reliever Roll-On for CGMP Violations
Pharma-Natural Inc. is recalling Army Health Pain Reliever Roll-On bottles due to manufacturing process violations. The product was distributed in Florida and Texas.
Product
ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On, 2.5 FL OZ (73ML) roll on bottle, Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00408 6.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2034-2019·2019-07-31
Siemens Artis zeego X-ray Generator Recall for Power Supply Tolerance Issue
Siemens Medical Solutions is recalling 117 Artis zeego units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Product
Artis zeego, Model Number 10280959
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2062-2019·2019-07-31
Merge PACS Software Recalled for Mammography Image Display Errors
Merge Healthcare is recalling specific versions of Merge PACS software because mammography images may not display in the correct reverse chronological order.
Product
Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2032-2019·2019-07-31
Siemens Artis zee floor MN X-ray generator recall
Siemens is recalling 23 Artis zee floor MN units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Product
Artis zee floor MN, Model Number 10094142
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1495-2019·2019-07-31
FDA Recalls Oliver's Harvest CBD+Lidocaine Cream for Manufacturing Violations
Pharma-Natural Inc. is recalling Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.
Product
Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief (Lidocaine HCL 4%) Topical Analgesic Cream, 4 OZ (113.4 g) bottle with pump, Distributed by: Coast to Coast Natural, Inc., Wellington, FL 33414, NDC 63766-119-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1988-2019·2019-07-31
Abbott Immunoglobulin A Diagnostic Assay Recalled for Instruction Manual Errors
Abbott Laboratories is recalling 12,995 Immunoglobulin A diagnostic kits because the instructions for use contained errors in the reagents and specimen handling sections.
Product
Immunoglobulin A is an in vitro diagnostic assay for the quantitative determination of immunoglobulin A in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1994-2019·2019-07-31
Abbott Apolipoprotein B Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 2,273 Apolipoprotein B in vitro diagnostic kits because the Instructions for Use (IFU) required updates to reagent and specimen handling sections.
Product
Apolipoprotein B is an in vitro diagnostic assay for the quantitative determination of apolipoprotein B in human serum or plasma. Antibodies to apolipoprotein B combine with apolipoprotein B in the sample to form insoluble immune complexes. The immune complexes cause an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2008-2019·2019-07-31
Becton Dickinson Recalls 3mL Safety-Lok Syringes Due to Incorrect Scale Markings
Becton Dickinson is recalling 428,800 3mL Safety-Lok Syringes because the scale markings were printed incorrectly, resulting in missing or partially printed numbers and lines.
Product
3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
Category
Medical Device
Distribution
13 states
ModerateFDA (Devices)·Z-2020-2019·2019-07-31
Siemens AXIOM Artis dFC X-ray Generator Recall for Power Supply Issue
Siemens is recalling 148 AXIOM Artis dFC units because a power supply defect may cause the X-ray generator to fail during procedures.
Product
AXIOM Artis dFC, Model Number 7412807
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1493-2019·2019-07-31
Pharma-Natural Recalls AbeeMed Cream Due to Manufacturing Violations
Pharma-Natural Inc. is recalling AbeeMed cream because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%), 2 OZ jar, Manufactured exclusively for: Cas, P.O. Box 520248, Miami, FL 33152, UPC 8 50993 00402 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1501-2019·2019-07-31
Lido E.R. Lidocaine Cream Recalled for Manufacturing Violations
Pharma-Natural Inc. is recalling Lido E.R. Lidocaine Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.
Product
Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream, 4 oz (113 g) jar, Distributed by Diabetic Supply of Suncoast, Inc., P.O. Box 2102, Vega Alta, PR 00692, NDC 63788-115-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1990-2019·2019-07-31
Abbott Immunoglobulin M Diagnostic Assay Recalled for Instruction Manual Errors
Abbott Laboratories is recalling 9,586 Immunoglobulin M diagnostic kits because the instructions for use contained errors in the reagents and specimen handling sections.
Product
Immunoglobulin M is an in vitro diagnostic assay for the quantitative determination of immunoglobulin M in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1995-2019·2019-07-31
Abbott Transferrin Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 22,359 Transferrin in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
Transferrin is an in vitro diagnostic assay for the quantitative determination of transferrin in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1516-2019·2019-07-31
Amneal Recalls Methylergonovine Maleate Tablets Due to Foreign Tablet Presence
Amneal Pharmaceuticals is recalling specific lots of Methylergonovine Maleate tablets because a Promethazine tablet was found in a bottle.
Product
Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC 69238-1605-02) and b) 28 count bottles (NDC 69238-1605-08)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1497-2019·2019-07-31
Pharma-Natural Recalls GENCONTUSS Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 3,000 bottles of GENCONTUSS cough syrup because it was manufactured with current good manufacturing practice violations.
Product
GENCONTUSS — GENCONTUSS (CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1506-2019·2019-07-31
Pharma-Natural Recalls NEOGEN-D Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 2,052 bottles of NEOGEN-D cough syrup because the product was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
NEOGEN-D (Dextromethorphan HBr, 30 mg; Guaifenesin, 200 mg; Phenylephrine HCl, 7.5 mg) in each 5 mL tsp, Raspberry Flavor, 16 fl oz (473 mL) bottle, Manufactured in the USA for Kramer Novis, San Juan, PR 00917, NDC 52083-699-16.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1991-2019·2019-07-31
Abbott Apolipoprotein A1 Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 2,112 Apolipoprotein A1 assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
Apolipoprotein A1 is an in vitro diagnostic assay for the quantitative determination of apolipoprotein A1 in human serum or plasma. Antibodies to apolipoprotein A1 combine with apolipoprotein A1 in the sample to form insoluble immune complexes. The immune complexes cause an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1499-2019·2019-07-31
Pharma-Natural Recalls LidoAID Gel Due to Manufacturing Violations
Pharma-Natural Inc. is recalling LidoAID topical analgesic gel because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
LidoAID (Lidocaine HCL 4%) portable pain relieving TOPICAL ANALGESIC GEL, 0.17 Oz (4 g) roll on bottle, Distributed by: Diabetic Supply of Suncoast, Inc., dba Advocate Diabetes, PO Box 2102, Vega Alta, PR 00692, NDC 63788-114-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1505-2019·2019-07-31
Pharma-Natural Recalls SORBUGEN Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 7,392 bottles of SORBUGEN cough syrup because the product was manufactured with current good manufacturing practice violations.
Product
SORBUGEN — SORBUGEN (DEXTROMETHORPHAN HYDROBROMIDE, GLYCEROL GUAIACOLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2001-2019·2019-07-31
Terumo Sur-vet Needle Recall Due to Potential Loss of Package Integrity
Terumo Medical Corporation is recalling 440,000 Sur-vet Needles due to a potential loss of package integrity that may compromise sterility.
Product
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220
Category
Medical Device
Distribution
12 states
ModerateFDA (Devices)·Z-1993-2019·2019-07-31
Abbott Haptoglobin Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 5,694 Haptoglobin Assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
The,K -ASSAY HP assay is intended for the quantitative determination of human haptoglobin by immunoturbidimetric assay. The antiserum used in the kit was produced against purified human haptoglobin. The haptoglobin antibody interacts with the haptoglobin in the serum forming…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2024-2019·2019-07-31
Siemens AXIOM Artis dFA Recalled for Power Supply Tolerance Issue
Siemens is recalling 39 AXIOM Artis dFA units because a power supply issue may cause generator failure, preventing X-ray production during procedures.
Product
AXIOM Artis dFA, Model Number 7555373
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2006-2019·2019-07-31
Terumo 30G Needle Recall Due to Potential Sterility Compromise
Terumo Medical Corporation is recalling 81,000 30G needles due to a potential loss of package integrity that may compromise sterility.
Product
Terumo Needle, 30G x 1/2", Product Code NN3013R
Category
Medical Device
Distribution
12 states
ModerateFDA (Devices)·Z-1998-2019·2019-07-31
Terumo Sur-vet Needle Recall Due to Potential Loss of Package Integrity
Terumo Medical Corporation is recalling 729,000 Sur-vet Needles because a potential loss of package integrity may compromise the sterility of the product.
Product
Terumo Sur-vet Needle, 20G x 1", Product Code 100204
Category
Medical Device
Distribution
12 states
ModerateFDA (Drugs)·D-1508-2019·2019-07-31
FDA Recalls Temozolomide Capsules Due to Cross-Contamination Risk
Deva Holding AS is recalling Temozolomide capsules because manufacturing deviations allowed possible cross-contamination with beta-lactam products.
Product
TEMOZOLOMIDE — TEMOZOLOMIDE (TEMOZOLOMIDE)
Category
Drug
Distribution
Distributed nationwide