State

New Hampshire product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46976–47000 of 78307

HighFDA (Devices)·Z-1390-2017·2017-03-08
Cook Inc. Recalls Flexor Radial Access Sets Due to Blood Loss Reports
Cook Inc. is recalling 41,975 Flexor Radial Access Sets because a specific hemostatic valve design is associated with increased reports of blood loss.
Product
Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1385-2017·2017-03-08
Merge Healthcare Recalls Unity PACS Software Due to Image Error
Merge Healthcare is recalling Unity PACS software versions 11.0 and 11.0.1 because the software fails to add the correct tomo image.
Product
DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1386-2017·2017-03-08
Maquet CARDIOSAVE IABP Li-Ion Battery Recall Due to Venting Risk
Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.
Product
CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 Product Usage: The CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1253-2017·2017-03-08
Phadia Recalls EliA Sample Diluent Due to Liquid Level Detection Issues
Phadia US Inc is recalling EliA Sample Diluent because liquid level detection problems in Phadia 250 instruments caused erroneous test results.
Product
EliA Sample Diluent, Article number, 83-1023-01
Category
Medical Device
Distribution
26 states
ModerateFDA (Drugs)·D-0508-2017·2017-03-08
Dr. Reddy's Recalls Zenatane Capsules for Dissolution Failure
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) 30 mg capsules because they failed to meet dissolution specifications.
Product
Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0502-2017·2017-03-08
Sun Pharmaceutical Recalls Alfuzosin Hydrochloride Tablets Due to Foreign Matter
Sun Pharmaceutical Industries is recalling specific lots of Alfuzosin Hydrochloride Extended-release Tablets because a consumer complaint identified a broken piece of wire rope embedded in a tablet.
Product
ALFUZOSIN HYDROCHLORIDE — ALFUZOSIN HYDROCHLORIDE (ALFUZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2017·2017-03-08
Cyclosporine Capsules Recalled for Impurity Specification Failures
Amerisource Health Services is recalling 454 cartons of Cyclosporine Capsules, 100 mg, due to failed impurity specifications.
Product
CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0506-2017·2017-03-08
Dr. Reddy's Recalls Zenatane Capsules for Dissolution Failure
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The affected lot is distributed nationwide.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1395-2017·2017-03-08
MED-EL SONNET Mini Battery Pack Cable Recall for Welding Defect
MED-EL is recalling 538 SONNET Mini Battery Pack Cables because the compartment lock was not firmly welded to the housing.
Product
SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery Pack, which is an external battery pack used to power one MED-EL SONNET control unit. It can be worn on the upper body or the hip using different SONNET Mini…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1256-2017·2017-03-08
Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias
Siemens is recalling specific Calibrator A kits due to confirmed negative bias and potential calibration failures for the FT4 assay on certain ADVIA Centaur systems.
Product
Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0507-2017·2017-03-08
Dr. Reddy's Recalls Zenatane Capsules Due to Dissolution Failures
Dr. Reddy's Laboratories is recalling specific lots of Zenatane (isotretinoin) 20 mg capsules because they failed to meet dissolution specifications.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1396-2017·2017-03-08
McKesson Radiology PACS Software Recall for Potential Missing Images
McKesson Medical Imaging is recalling McKesson Radiology 12.2 PACS software due to a defect that may cause missing images or stuck imports.
Product
McKesson Radiology 12.2 - Picture Archive Communication System (PACS)
Category
Medical Device
Distribution
14 states
ModerateFDA (Devices)·Z-1394-2017·2017-03-08
BD AffirM VPIII Microbial Identification Test Recalled for Invalid Results
Becton Dickinson is recalling specific lots of the BD AffirM VPIII Microbial Identification Test because blue speckles or fibers may cause invalid test results.
Product
BD AffirM VPIII Microbial Identification Test
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1254-2017·2017-03-08
Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias
Siemens recalls ADVIA Centaur Calibrator A kits due to negative bias in FT4 assays and potential calibration failures on specific systems.
Product
Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0500-2017·2017-03-08
Allegiant Health Recalls HealthA2Z Chewable Aspirin Due to Rubber Particles
Allegiant Health is recalling HealthA2Z Chewable Aspirin 81 mg because rubber particles were found in the bulk product.
Product
HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg, Orange Flavor, 36 Chewable Tablets, a) packaged in 36-count bottle [UPC Code 369168288362 (FP0545)], b) bulk product (6K28817), OTC, Manufactured by: Allegiant Health Deer Park, NY 11729
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0504-2017·2017-03-08
Perrigo Recalls Salicylic Acid Cream Due to Organic Impurity
L. Perrigo Company is recalling Salicylic Acid Cream, 6%, due to an out-of-specification organic impurity. The FDA classified this as a Class III recall.
Product
Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0503-2017·2017-03-08
Perrigo Recalls Salicylic Acid Shampoo Due to Organic Impurity
L. Perrigo Company is recalling Salicylic Acid Shampoo, 6%, because the active ingredient failed impurity specifications.
Product
Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0509-2017·2017-03-08
Dr. Reddy's Recalls Zenatane Capsules Due to Dissolution Failure
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The recall covers 4,404 cartons distributed nationwide.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V149000·2017-03-07
Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Driveshaft Welding Defect
Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because a driveshaft bracket may not be properly welded, posing a fire risk in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V145000·2017-03-07
Zero Motorcycles Recalls 2017 S, DS, and FXS Models for ABS Defect
Zero Motorcycles is recalling 2017 S, DS, and FXS motorcycles because the Anti-Lock Braking System may function improperly, increasing crash risk.
Product
ZERO — ZERO S, DS, FXS
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·17105·2017-03-07
Craftsman Portable Table Saws Recalled for Stand Collapse Injury Hazards
Rexon is recalling about 46,000 Craftsman portable table saws sold at Sears because the stand can collapse, posing laceration and impact injury risks.
Product
Craftsman portable table saws
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V148000·2017-03-07
Mercedes-Benz Metris Recall for Non-Functioning Blind Spot Monitoring
Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vans because the Blind Spot Monitoring system does not work due to incompatible parts.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17E014000·2017-03-07
H&H Sports Protection Recalls TORC T-55 V2 Motorcycle Helmets
H&H Sports Protection is recalling TORC T-55 V2 half helmets because they may not adequately protect the wearer or stay secured during a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17733·2017-03-07
L.L. Bean Recalls Snowshoes Due to Plastic Frame Breakage Hazard
L.L. Bean is recalling Adventure Adjustable Snowshoes because the plastic deck can weaken and break, posing a fall hazard. No injuries have been reported.
Product
Snowshoes and snowshoe packages
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V147000·2017-03-07
Keystone Recalls 2017 Cougar and Laredo Trailers for Smoke Detector Defect
Keystone is recalling 2017 Cougar and Laredo recreational trailers that may have two carbon monoxide detectors instead of a smoke detector, increasing fire injury risk.
Product
KEYSTONE — KEYSTONE COUGAR, LAREDO
Category
Vehicle
Distribution
Distributed nationwide