State
73,806 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.
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.
Lannett Company is recalling 8,324 bottles of Hydroxyzine Hydrochloride Syrup because cleaning procedures caused out-of-specification results for unknown impurities.
Teva Pharmaceuticals USA is recalling 53,451 bottles of Metoprolol Succinate Extended Release Tablets 50 mg because routine stability testing revealed out-of-specification dissolution results.
Philips is recalling DigitalDiagnost software for stationary X-ray systems due to intermittent stitching interruptions and incorrect baseline data on the system CD.
Lupin Pharmaceuticals is recalling 2,712 bottles of Fluocinolone Acetonide Topical Solution because stability testing showed total impurities exceeded specifications.
BioMerieux is recalling 42 units of NucliSENS Magnetic Extraction Reagents because data loggers indicated one shipment experienced low temperatures that may impact performance.
Ecolab Inc is recalling specific lots of Disposable Accessory Kits, 3-Arm, due to potential pouch seal defects that could compromise sterility.
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to software anomalies affecting startup, motion control, and image acquisition.
Upsher Smith Laboratories is recalling 29,080 bottles of Bumetanide 2 mg tablets because the product failed impurity specifications for an unspecified degradation product.
bioMerieux is recalling 8 BACT/ALERT VIRTUO systems because firmware version R2.0 allows calibration standards to be moved, potentially causing anomalies if not returned to designated locations.
Micro-Tech (Nanjing) Co., Ltd. is recalling 1,360 units of Single-Use Biopsy Forceps because the boxes contained Grasping Forceps instead of the labeled product.
Westlab Pharmacy is recalling 80 vials of Alprostadil 500 mcg/mL Injectable due to an incorrect product formulation. The recall covers nationwide distribution.
Fantasia Accessories is recalling about 22,500 children's slap bracelets sold at Target because the metal band can pierce the fabric cover, posing a laceration hazard.
RXQ Compounding LLC is recalling 395 vials of Lidocaine 1% + Epinephrine 1:100,000 injection solution because testing revealed the product was subpotent.
Stryker is recalling 389 Altrix Precision Temperature Management Systems due to frequent alarms and mechanical interference faults.
bioMerieux is recalling 151 BACT/ALERT VIRTUO systems with R2.0 firmware because a software feature may allow calibration standards to be left in incorrect positions, potentially causing anomalies.
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to reported software anomalies affecting startup, communication, and imaging functions.
Terumo is recalling 135 units of the VirtuoSaph Plus Endoscopic Vessel Harvesting System because one energy platform is not compatible with the device.
bioMerieux is recalling 516 BACT/ALERT VIRTUO systems with R2.0 firmware because a service feature may leave calibration standards in incorrect locations, potentially causing anomalies.
Ecolab is recalling specific lots of sterile instrument arm drapes for the Da Vinci Si system because seal wrinkles may compromise sterility.
Lupin Pharmaceuticals is recalling 6,752 bottles of Testosterone Topical Solution because the pump mechanism is not working.
Promise Pharmacy LLC is recalling Prednisolone and Gatifloxacin Ophthalmic Solution due to the presence of precipitate. The recall covers nationwide distribution.
Altec Industries is recalling 2009 LSS 60 and LSS 70 Elevator Aerial devices because the elevator riser assembly may crack and fail, increasing the risk of injury or death.
Hickory Springs is recalling specific school bus seats because bolts securing the seat pedestal to the floor may fracture, potentially increasing injury risk during a crash.
Thor Motor Coach is recalling 1,769 motorhomes because a damaged power distribution module may cause rear lights or turn signals to fail, increasing crash risk.
Volvo is recalling 2004-2019 VHD trucks with snow plow kits because the headlights can operate without other exterior lights, reducing visibility.