The Recall Desk

State

New Hampshire product recalls

72,940 recalls have nationwide distribution and so reach New Hampshire. 4,444 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,444
Critical
596
Severe
846
Most recent
2026-09-09

Of the 4,444 recalls naming New Hampshire we have scored against our rubric, 596 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 846 (19%) are Severe.

Which agencies issued them

These figures cover only the 4,444 recalls whose distribution notice names New Hampshire specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4376–4400 of 77384

  • CriticalFDA (Devices)·Z-0451-2026·2025-11-19

    Orthopedic and spine kits recalled over cracked anesthesia circuit tubing

    Medline is recalling ortho spine, total joint and kyphoplasty convenience kits after complaints of anesthesia circuit leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0434-2026·2025-11-19

    Detachable brain aneurysm coils recalled because they may fail to detach

    Cerenovus is recalling 12,004 CEREPAK Detachable Coil System units because the coils may fail to detach, which could result in hemorrhagic and ischemic stroke. The FDA classified it Class I.

    Product
    CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM 3MM X 5.4 CM/FCX100305, UNIFORM 3.5MM X 6.6 CM/FCX100356, UNIFORM 4MM X 7.5 CM/FCX100407, UNIFORM 4MM X 11.5 CM/FCX100412, UNIFORM 5MM X 9.7 CM/FCX100509, UNIFORM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0443-2026·2025-11-19

    Breathing kits recalled over cracks in the expandable anesthesia tubing

    Medline is recalling the latex-free Breathing Kit DYNJ10550 after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; BREATHING KIT-LF DYNJ10550
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0449-2026·2025-11-19

    Expandable anesthesia circuits recalled over cracks causing leaks in tubing

    Medline is recalling the 120-inch latex-free ExtendFlex anesthesia circuit after complaints of leaks caused by cracks in the expandable tubing. The FDA has classified it Class I.

    Product
    Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0460-2026·2025-11-19

    Urodynamics tables recalled over an inadequate weld on the backrest bracket

    Sonesta Medical is recalling 10 Sonesta 6210 video urodynamics procedure tables because an inadequate weld on the backrest bracket can result in the backrest dropping.

    Product
    Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description: Sonesta 6210 - Procedure table designed for full fluoroscopic imaging of the urinary tract during video Urodynamics procedures. Component: N/A
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·H-0181-2026·2025-11-19

    Nutra Calm supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 452 bottles of Nutra Calm capsules because the product contains magnesium salicylate.

    Product
    Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku: PB248
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0493-2026·2025-11-19

    Food allergen panels recalled over barcodes causing wrong tube scanning order

    Siemens Healthcare Diagnostics is recalling 28 units of Food Panel 3 Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.

    Product
    Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0489-2026·2025-11-19

    Hematology analyzers recalled because saturation flags may not be applied

    Abbott Laboratories is recalling 833 Alinity hq Analyzers because a software issue means the system does not visibly flag results when saturation is present, which may give incorrect results.

    Product
    Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number: 09P68-01 Software Version: 5.0 to 5.10.1 for OUS, 5.7 and 5.10.1 in the US Product Description: Alinity hq Analyzer Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0494-2026·2025-11-19

    Nasal feeding tubes recalled from a second lot for possible occlusion

    Applied Medical Technology is recalling NutraGlide 5 F-6 F x 55 nasal feeding tubes with stylet and ENfit, REF NFT-05055-I, from one lot because the tube may be occluded.

    Product
    Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0452-2026·2025-11-19

    Lithotripsy transducers recalled over startup failures and handpiece temperature rise

    Olympus is recalling 1,528 ShockPulse Lithotripsy Transducers because the device may fail to start or stop shortly after starting, and the handpiece body may heat up during clinical use.

    Product
    Brand Name: Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer Model/Catalog Number: SPL-T Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse tra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0476-2026·2025-11-19

    Reprocessed vessel sealers recalled over residual material that may dislodge

    Medline is recalling 57,244 reprocessed LigaSure Maryland Jaw sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.

    Product
    Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2026·2025-11-19

    Oxygen concentrator batteries recalled over a chip that can stop oxygen

    Philips Respironics is recalling 56 SimplyGo Mini standard battery kits because a defective chip can make the battery fail, shutting down the concentrator and stopping oxygen delivery.

    Product
    SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2026·2025-11-19

    CARESCAPE ONE monitors recalled over batteries that fail to hold charge

    GE Healthcare is recalling 5,935 CARESCAPE ONE patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.

    Product
    CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2026·2025-11-19

    Five millimetre blunt tip sealers recalled over trapped residual material

    Medline is recalling two reprocessed LigaSure Blunt Tip sealer/dividers, 5 mm x 37 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0183-2026·2025-11-19

    Tense-X supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 253 bottles of Tense-X capsules because the product contains magnesium salicylate.

    Product
    Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0477-2026·2025-11-19

    Maryland jaw sealers 44 cm recalled over trapped residual material

    Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0498-2026·2025-11-19

    Long nasal feeding tubes recalled from one lot for possible occlusion

    Applied Medical Technology is recalling NutraGlide 6 F-8 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.

    Product
    Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0182-2026·2025-11-19

    Dietary supplement recalled because it contains magnesium salicylate

    Professional Botanicals is recalling 430 bottles of Total Comfort capsules because the product contains magnesium salicylate.

    Product
    Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0486-2026·2025-11-19

    VATS lobectomy stapler boxes recalled over a malformed cover tube press

    Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.

    Product
    Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0499-2026·2025-11-19

    Ceiling X-ray tube supports recalled over a shaft that may break

    Shimadzu is recalling 1,766 ceiling type X-ray tube supports, models CH-200 and CH-200M, because the mounting shaft may break and the tube assembly could come off.

    Product
    Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The ceiling type x-ray tube support CH-200 is used to hold the X-ray tube and collimator to position the X-ray tube unit. This unit is used for radiographic ex
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0469-2026·2025-11-19

    Impact vessel sealers recalled over residual material that may dislodge

    Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.

    Product
    Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2026·2025-11-19

    Mobile X-ray systems recalled over bolts that may loosen or fracture

    NeuroLogica is recalling 236 GM85 digital mobile X-ray systems because the four M5 bolts securing the tube head unit to the arm may loosen or fracture from metal fatigue.

    Product
    GM85 Digital Mobile X-ray imaging System; Model Number: GM85;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V800000·2025-11-19

    McNeilus Recalls 2024-2025 Volterra ZSL Trucks Due to Software Error

    McNeilus is recalling 2024-2025 Volterra ZSL side loader garbage trucks because a software error may cause grabber fingers to move without operator input, posing a risk of injury or crash.

    Product
    MCNEILUS — MCNEILUS VOLTERRA ZSL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0474-2026·2025-11-19

    Blunt tip sealers 44 cm recalled over trapped residual material

    Medline is recalling 1,446 reprocessed LigaSure Blunt Tip sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.

    Product
    Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 44cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
    Category
    Medical Device
    Distribution
    Distributed nationwide