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.

34101–34125 of 78223

HighFDA (Devices)·Z-2273-2019·2019-08-21
Siemens SOMATOM Edge Plus CT Systems Recalled for Software Issues
Siemens is recalling SOMATOM Edge Plus CT systems due to four safety-related software issues in syngo.CT version VB10A that may cause scan aborts.
Product
SOMATOM Edge Plus, Model Number 10267000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2257-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x120 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x120, Item Number 19672 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2247-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x100 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x100, Item Number 19668 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2251-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x85 due to a manufacturing flaw in the sterile barrier system. The devices were distributed in the US and internationally.
Product
Go-EZ Screw 6.5x85, Item Number 19665 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2272-2019·2019-08-21
Siemens SOMATOM Confidence CT Systems Recalled for Software Safety Issues
Siemens Medical Solutions is recalling SOMATOM Confidence CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Confidence, Model Number 10590100 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2269-2019·2019-08-21
Siemens CT Systems Recalled for Software Issues Causing Scan Aborts
Siemens is recalling SOMATOM Definition Edge CT systems due to four safety-related software issues in syngo.CT version VB10A that may result in scan aborts.
Product
SOMATOM Definition Edge, Model Number 10590000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2279-2019·2019-08-21
BD Vacutainer Fluoride Tubes Recalled Due to Missing Preservative Additive
Becton Dickinson is recalling 247,000 blood alcohol test tubes because they lack the required fluoride additive, which may cause inaccurate test results if samples are stored for more than two days.
Product
BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol determinations
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2274-2019·2019-08-21
Siemens SOMATOM Force CT Systems Recalled for Software Scan Abort Issues
Siemens Medical Solutions is recalling SOMATOM Force CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Force, Model Number 10742326 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2255-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x105 (Item 19669) due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x105, Item Number 19669 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1990-2019·2019-08-21
Entenmann's Little Bites Cookies Recalled for Possible Plastic Pieces
BIMBO Bakeries USA Inc. is recalling 160,000 boxes of Entenmann's Little Bites Soft Baked Cookies due to a manufacturing failure that may have introduced small plastic pieces into the product.
Product
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5 pouches per package, package type is carton, units per case 12
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-2249-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x95 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x95, Item Number 19667 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2275-2019·2019-08-21
NeuroLogica HS70A Ultrasound Systems Recalled for Probe Overheating Risk
NeuroLogica is recalling HS70A Diagnostic Ultrasound Systems due to a potential risk of probes overheating when users decrease the Doppler Sample Volume size in Doppler Only mode.
Product
HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00.09, 1.00.10, 1.00.11, 1.00.12
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2239-2019·2019-08-21
BioPro K-Wire HBS Sterile Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 17 units of K-Wire HBS Sterile due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V613000·2019-08-21
McLaren Recalls 2018-2019 Senna Vehicles for Engine Harness Chafing Defect
McLaren is recalling 2018-2019 Senna vehicles because the engine harness may chafe against a heat shield, potentially causing engine power loss or stalling.
Product
MCLAREN — MCLAREN SENNA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2258-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x38 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x38, Item Number 19655 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2276-2019·2019-08-21
NeuroLogica WS80A Diagnostic Ultrasound System Recalled for Probe Overheating Risk
NeuroLogica is recalling WS80A Diagnostic Ultrasound Systems because probes may overheat when users decrease the Doppler Sample Volume size in Doppler Only mode.
Product
WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01.06, 3.01.07, 3.01.08, 3.01.09, 4.00.08, 4.00.09, 4.00.10, 4.00.11, 4.01.00, 4.01.01, 4.01.02, 4.01.03, 4.01.04, 4.01.05, 4.01.06, 4.01.07…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1844-2019·2019-08-21
Macleods Pharma Recalls Tamsulosin Hydrochloride Capsules for Dissolution Failures
Macleods Pharma USA Inc is recalling Tamsulosin Hydrochloride Capsules because they failed to meet dissolution specifications.
Product
TAMSULOSIN HYDROCHLORIDE — TAMSULOSIN HYDROCHLORIDE (TAMSULOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1730-2019·2019-08-21
US Pharmaceuticals Recalls Adult Glycerin Suppositories for Water Quality Issues
US Pharmaceuticals is recalling 880 cases of Adult Glycerin Suppositories because purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
Adult Glycerin Suppositories, Package Size 100-count suppositories, Distributed By: Walgreen Co. 200 Wilmot Rd. Deerfield, IL 60015. NDC#0363-0441-00
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1739-2019·2019-08-21
US Pharmaceuticals Recalls Kool Comfort Cooling Pain Relief Due to Water Quality Issues
US Pharmaceuticals is recalling Kool Comfort Cooling Pain Relief because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
Kool Comfort Cooling Pain Relief, 5% Menthol, Packaged in a) 3 OZ./85 g (UPC 0 52301 35903 5); b) 4 OZ/ 113 g (UPC 0 52301 36504 3); c) 32 OZ/ 907 g (UPC 0 52301 36532 6); d) 16 OZ/ 454 g (UPC 0 52301 36516 6); e) 128 OZ/ 3629 g (UPC 0 52301 36512 8) Manufactured for: Dee Cee…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1733-2019·2019-08-21
US Pharmaceuticals Recalls Hydrocortisone Cream Due to Water Quality Issues
US Pharmaceuticals Inc. is recalling 305 cases of Maximum Strength Hydrocortisone Cream because the purified water used in manufacturing failed quality tests.
Product
MAXIMUM STRENGTH HYDROCORTISONE CREAM — MAXIMUM STRENGTH HYDROCORTISONE CREAM (HYDROCORTISONE CREAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1734-2019·2019-08-21
US Pharmaceuticals Recalls Hydrocortisone Cream Due to Water Quality Issues
US Pharmaceuticals is recalling 651 cases of Maximum Strength Hydrocortisone Cream because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
MAXIMUM STRENGTH HYDROCORTISONE CREAM — MAXIMUM STRENGTH HYDROCORTISONE CREAM (HYDROCORTISONE CREAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1740-2019·2019-08-21
US Pharmaceuticals Recalls Wonder Freeze Pain Gel Due to Water Quality Issues
US Pharmaceuticals is recalling Wonder Freeze Pain Relieving Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
Wonder Freeze Pain Releiving Gel with ILEX, Menthol 5%, packaged in a) 3 OZ /85 g (UPC 0 99528 35903 5); b) 4 OZ / 113 g (UPC 0 99528 31504 8); c) 16 OZ / 454 g (UPC 0 99528 31516 1); Manufactured For: Wonder Laboratories, 115 S.C.T. Ct., White House TN. 37188.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1727-2019·2019-08-21
US Pharmaceuticals Recalls Children's Glycerin Suppositories for Water Quality Issues
US Pharmaceuticals is recalling 76 cases of Children Glycerin Suppositories due to out-of-specification results in the purified water used during manufacturing.
Product
Children Glycerin Suppositories Laxative for ages 2 to 5. Package Size 25-count.Distributed by Walgreen CO. 200 Wilmot Rd. Deerfield IL 60015. NDC#0363-0440-25,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1741-2019·2019-08-21
US Pharmaceuticals Recalls CRYO-273 Cold Pain Gel Due to Water Quality Issues
US Pharmaceuticals is recalling CRYO-273 Cold Pain Relieving Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
CRYO-273 Cold Pain Relieving Gel 128 FL. OZ. Distributed By: CRYO-273.com Tampa, FL 33629. UPC 8 15290 01550 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1736-2019·2019-08-21
CVS Health Glycerin Suppositories Recalled for Water Quality Issues
US Pharmaceuticals is recalling CVS Health Glycerin Suppositories because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Product
CVS Health Glycerin Suppositories, 100- count box, Distributed by:Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895. UPC 0 50428 42738 5
Category
Drug
Distribution
Distributed nationwide