The Recall Desk

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.

47901–47925 of 78307

  • ModerateFDA (Devices)·Z-0736-2017·2016-12-21

    C.R. Bard Recalls 70cc Piston Syringes Due to Package Defect

    C.R. Bard is recalling 70cc Piston Syringes because a package slit defect may compromise product sterility.

    Product
    BARD¿ 70cc Piston Syringe with Catheter Tip, Luer Adapter and Cap, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0754-2017·2016-12-21

    Olympus HF Cable WA00014A Recalled for Software Malfunction

    Olympus Corporation of the Americas is recalling 494 HF Cable WA00014A units due to a software malfunction that may cause incorrect error codes to be generated or displayed.

    Product
    HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0756-2017·2016-12-21

    Recall of Sterile Specimen Containers Due to Packaging Defect

    Covidien LLC is recalling 5,187,100 sterile specimen containers because a packaging defect compromised the sterility of the outer surface.

    Product
    Covidien Precision Specimen Container- 4 oz (118 mL), Plastic Screw Top Cap, OR Packaged, Sterile Item Code: 17099
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0737-2017·2016-12-21

    C.R. Bard Recalls Piston Syringes Due to Package Defect Risk

    C.R. Bard is recalling specific lots of 60cc Piston Syringes because a package slit defect may compromise product sterility.

    Product
    BARD¿ Piston Syringe, 60cc, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are included. BARD¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0742-2017·2016-12-21

    Siemens SOMATOM Definition AS CT Systems Recalled for Software Bug Fixes

    Siemens Medical Solutions USA is recalling 104 SOMATOM Definition AS CT systems to install software and firmware updates that fix bugs and improve performance.

    Product
    SOMATOM Definition AS System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0744-2017·2016-12-21

    Siemens SOMATOM Definition Edge CT Systems Recalled for Software Bug Fixes

    Siemens Medical Solutions is recalling 104 SOMATOM Definition Edge CT systems to install a software update that fixes bugs and improves performance.

    Product
    SOMATOM Definition Edge System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0738-2017·2016-12-21

    C.R. Bard Recalls BARDIA 60cc Piston Irrigation Syringes Due to Package Defect

    C.R. Bard is recalling BARDIA 60cc Piston Irrigation Syringes because a slit defect in the packaging may compromise product sterility.

    Product
    BARDIA¿ 60cc Piston Irrigation Syringe, Sterile, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0740-2017·2016-12-21

    BD Recalls Spinal Anesthesia Trays Due to Incorrect Labeling

    Becton Dickinson is recalling 4,500 BD Spinal Anesthesia Trays because a small number were incorrectly labeled as Epidural Trays.

    Product
    BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perform the spinal anesthesia procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0769-2017·2016-12-21

    Natus neoBLUE Phototherapy Systems Recalled for Fiberoptic Pad Failure

    Natus Medical is recalling neoBLUE blanket LED Phototherapy Systems due to early failure of fiberoptic pads, which can cause discoloration and melting at the connector.

    Product
    Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides phototherapy underneath the infant and can be used in a bassinet, open bed, radiant warmer, incubator, or while holding the infant. Affected systems including: 1) Updated light boxes (serial number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0740-2017·2016-12-21

    Cargill Recalls Quali Fry Premium Buttery Pan and Grill Oil

    Cargill is recalling Quali Fry Premium Buttery Pan and Grill Oil because it contains excessive amounts of TBHQ and dimethyl polysiloxane.

    Product
    QUALI FRY PREMIUM BUTTERY PAN AND GRILL, ARTIFICIALLY FLAVORED OIL, NET/NETO 1 GAL (3.79 L) INGREDIENTS: SOYBEAN OIL, HYDROGENATED SOYBEAN OIL***TBHQ***DIMETHYLPOLYSILOXANE***CONTAINS: SOY, UPC 7 58108 45416 3
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0757-2017·2016-12-21

    Pentax Ultrasound Video Bronchoscope Recalled for Incorrect Instructions

    Pentax of America Inc. is recalling 113 Ultrasound Video Bronchoscopes because they shipped with outdated instructions for use.

    Product
    Ultrasound Video Bronchoscope The EB-1970UK, Ultrasound Video Bronchoscope, is intended to provide optical visualization of, ultrasonic visualization of, and therapeutic access to, the Pulmonary Track including but not restricted to organs, tissues, and subsystem: Nasal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0750-2017·2016-12-21

    Roche Recalls LightMix Zika rRT-PCR Test Due to False Positive Risk

    Roche Molecular Systems is recalling the LightMix Zika rRT-PCR Test because the software algorithm may occasionally report false positive results.

    Product
    LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is a real-time RT-PCR test intended for the qualitative detection of RNA from the Zika virus in serum or EDTA plasma from individuals meeting CDC Zika virus clinical criteria (e.g., clinical signs and symptoms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0205-2017·2016-12-21

    Jubilant Cadista Recalls Methylprednisolone Tablets Due to Incorrect Expiration Date Labeling

    Jubilant Cadista Pharmaceuticals is recalling 1,512 bottles of Methylprednisolone Tablets, USP, 16 mg, because the expiration date is printed incorrectly as 02/0218 instead of 02/2018.

    Product
    Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-003-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V913000·2016-12-20

    Volkswagen Recalls 2009-2010 Models for ABS Control Unit Failure

    Volkswagen is recalling 2009-2010 Jetta, GTI, Golf, and Audi A3 vehicles because the ABS control unit may fail, potentially causing loss of vehicle control.

    Product
    AUDI — AUDI, VOLKSWAGEN A3, JETTA SPORTWAGEN, JETTA, GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17056·2016-12-20

    Zebra Thermal Printer Power Supply Units Recalled for Fire Hazard

    Zebra Technologies is recalling approximately 166,000 power supply units for thermal printers due to a fire hazard caused by overheating and corrosion.

    Product
    Power supply units for Zebra brand thermal printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V912000·2016-12-20

    C&M Recalls 2016 Trailers with Missing Front Reflex Reflectors

    C&M Trailers is recalling 670 model year 2016 boat, jet ski, and utility trailers because they may be missing front reflex reflectors, which could make them harder to see.

    Product
    C&M — C&M BOAT TRAILER, JET SKI TRAILER, UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V914000·2016-12-20

    BMW, MINI, and Rolls-Royce Recall for Air Bag Initiator Defect

    BMW is recalling 2016-2017 vehicles because seat-mounted air bag initiators may fail to ignite, preventing deployment and increasing injury risk.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE X1 SAV, 550I, M5, 535D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16C008000·2016-12-19

    Baby Trend Recalls Booster Seats Due to Harness Rivet Failure Risk

    Baby Trend is recalling specific Hybrid LX booster seats because a center adjuster rivet may break if used with children over 40 lbs, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V911000·2016-12-19

    Nissan Recalls Altima, Rogue, and Maxima for Air Bag Sensor Defect

    Nissan is recalling specific 2013-2016 Altima, Rogue, and Maxima vehicles because an incorrect air bag sensor may misclassify front passengers, increasing injury risk in crashes.

    Product
    NISSAN — NISSAN ALTIMA, ROGUE, MAXIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17055·2016-12-16

    LG Recalls Portable Air Conditioners Due to Fire Hazard

    LG Electronics is recalling about 466,000 portable air conditioners sold in the U.S. because they can overheat and cause fires.

    Product
    Portable Air Conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V906000·2016-12-16

    Toyota Recalls 2016 Avalon and 2017 Camry for Knee Air Bag Fastener Issue

    Toyota is recalling specific 2016 Avalon and 2017 Camry vehicles because the front passenger knee air bag may be attached with incorrect fasteners, which could affect deployment and increase injury risk.

    Product
    TOYOTA — TOYOTA AVALON, CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V910000·2016-12-16

    RAM ProMaster Recall: Side Air Bag Inflator May Fail to Ignite

    Chrysler is recalling 2017 RAM ProMaster vehicles because the seat-mounted side air bag inflator initiator may fail to ignite during a crash.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide