The Recall Desk

State

New Hampshire product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43501–43525 of 78300

  • SevereFDA (Drugs)·D-1141-2017·2017-09-20

    Centurion Labs Recalls Ninjacof-A Oral Solution Due to Microbial Contamination

    Centurion Labs is recalling Ninjacof-A oral solution due to potential B. cepacia contamination. Consumers should stop using the product and return it to the pharmacy.

    Product
    Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy Flavor, Manufactured for: Centurion Labs, LLC Birmingham, AL 35243 --- NDC 23359-033-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3523-2017·2017-09-20

    Rugby Tri-vitamin Liquid Recalled for B. cepacia Contamination

    The Harvard Drug Group is voluntarily recalling Rugby Tri-vitamin Liquid due to possible contamination with B. cepacia, which poses a risk of serious infection for vulnerable patients.

    Product
    Rugby Tri-vitamin Liquid, 1 2/3 oz (50 mL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3526-2017·2017-09-20

    Voluntary Recall of Major Ferrous Drops Due to B. cepacia Contamination

    The Harvard Drug Group is voluntarily recalling Major Ferrous Drops due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.

    Product
    Major Ferrous Drops, 1 2/3 oz (50 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1160-2017·2017-09-20

    Bella Pharmaceuticals Recalls Bevacizumab Syringes Due to Sterility Concerns

    Bella Pharmaceuticals is recalling 2,334 Bevacizumab prefilled syringes nationwide due to a lack of assurance of sterility.

    Product
    Bevacizumab Prefilled 30g and 31 gram 1.25mg/0.05mL Syringes, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3528-2017·2017-09-20

    Voluntary Recall of Major Poly-Vita Drops Due to B. cepacia Contamination

    The Harvard Drug Group is voluntarily recalling Major Poly-Vita Drops with Iron due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.

    Product
    Major Poly-Vita Drops with Iron, 1 2/3 oz (50 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1148-2017·2017-09-20

    Bella Pharmaceuticals Recalls Mannitol 20% Vials Due to Sterility Concerns

    Bella Pharmaceuticals is recalling Mannitol 20% 10 mL vials because the company cannot ensure the product is sterile.

    Product
    Mannitol 20%, 10 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3515-2017·2017-09-20

    Rugby Calcionate Syrup Recalled for Possible B. cepacia Contamination

    The Harvard Drug Group is voluntarily recalling Rugby Calcionate Syrup due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.

    Product
    Rugby Calcionate Syrup, One Pint (473 mL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3520-2017·2017-09-20

    Rugby Ferrous Sulfate Liquid Recalled for B. cepacia Contamination

    The Harvard Drug Group is voluntarily recalling Rugby Ferrous Sulfate Liquid due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.

    Product
    Rugby Ferrous Sulfate Liquid One Pint, (473 mL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1152-2017·2017-09-20

    Bella Pharmaceuticals Recalls Methylcobalamin Vials Due to Sterility Concerns

    Bella Pharmaceuticals is recalling 7 vials of Methylcobalamin 10mg due to a lack of assurance of sterility. The product was distributed nationwide in the United States.

    Product
    Methylcobalamin 10mg, (10mg/ml), 30 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3531-2017·2017-09-20

    Leader Liquid Vitamin D Supplement Recalled for B. cepacia Contamination

    Leader Liquid Vitamin D Supplement for Breastfed Infants is being voluntarily recalled due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.

    Product
    Leader Liquid Vitamin D Supplement for Breastfed Infants, 1 T oz (50 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1153-2017·2017-09-20

    Bella Pharmaceuticals Recalls Magnesium Chloride Vials Due to Sterility Concerns

    Bella Pharmaceuticals is recalling Magnesium Chloride 200mg vials because the company cannot ensure the product is sterile.

    Product
    Magnesium Chloride 200mg, 30m L vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1150-2017·2017-09-20

    Bella Pharmaceuticals Recalls Calcium Chloride Vials Due to Sterility Concerns

    Bella Pharmaceuticals is recalling specific lots of Calcium chloride 10% vials because the company cannot ensure the product is sterile.

    Product
    Calcium chloride 10%, 10 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3516-2017·2017-09-20

    Rugby Cerovite Liquid Recalled for Possible B. cepacia Contamination

    The Harvard Drug Group is voluntarily recalling Rugby Cerovite Liquid due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.

    Product
    Rugby Cerovite Liquid, 8 oz. 236ML
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3517-2017·2017-09-20

    Rugby Vitamin D3 Liquid Recalled for B. cepacia Contamination Risk

    The Harvard Drug Group is voluntarily recalling Rugby D 3 Vitamin Liquid due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.

    Product
    Rugby D 3 Vitamin Liquid, 400 IUI/1 mL, 1 and 2/3 oz., 50 mL
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V576000·2017-09-20

    Porsche Recalls Cayenne Models Due to Fuel Pump Flange Crack Risk

    Porsche is recalling specific 2003-2006 Cayenne models because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.

    Product
    PORSCHE — PORSCHE CAYENNE S, CAYENNE TURBO, CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1154-2017·2017-09-20

    Bella Pharmaceuticals Recalls L-Glutamine Vials Due to Sterility Concerns

    Bella Pharmaceuticals is recalling specific lots of L-Glutamine 100mg vials because the company cannot guarantee the product is sterile.

    Product
    L-Glutamine 100mg, 30 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V582000·2017-09-20

    Double K Recalls 2016-2017 Hometown Trolley Buses for Seat Belt Defect

    Double K is recalling 2016-2017 Hometown Trolley buses because the seat belt buckle may be stuck in the locked position, preventing the belt from latching.

    Product
    HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, MAINSTREET, VILLAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17228·2017-09-20

    DEMDACO Recalls Infant Bib and Bootie Sets Due to Choking Hazard

    DEMDACO is recalling about 1,500 infant bib and bootie sets because rattle attachments can detach, posing a choking hazard. No injuries have been reported.

    Product
    Infant bib and bootie sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3117-2017·2017-09-20

    Zimmer Biomet Recalls ROSA Surgical Device Foot Switches

    Zimmer Biomet is recalling 64 ROSA surgical device foot switches that may freeze or shut down during use.

    Product
    Herga foot switch, model 6289-WS, a component of the ROSA Robotized Stereotactic Assistant Surgical Device, Model 2.5.8. The firm name on the foot switch label is Herga Electric Limited, Bury, St. Edmunds, Suffolk IP32 6NN. ROSA Surgical Device is a computer-controlled…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V584000·2017-09-20

    Fleetwood Recalls 2013-2016 RVs Due to Battery Tray Weld Defect

    REV Recreation Group is recalling 2013-2016 Fleetwood Bounder and Southwind RVs because insufficient battery tray welds may cause the tray to separate, risking fire or injury.

    Product
    FLEETWOOD — FLEETWOOD BOUNDER, SOUTHWIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17227·2017-09-20

    John Deere Recalls D105 Lawn Tractors Due to Transmission Crash Hazard

    John Deere is recalling D105 lawn tractors and service transmissions because the transmission can fail, posing a crash hazard. No injuries have been reported.

    Product
    John Deere D105 lawn tractors and service part transmissions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3133-2017·2017-09-20

    Baxter Amia Automated Peritoneal Dialysis Set Recalled for Flow Issues

    Baxter Healthcare is recalling 164,700 units of Amia Automated Peritoneal Dialysis Sets due to increased customer complaints regarding flow and drain alerts.

    Product
    Baxter Amia Automated Peritoneal Dialysis Set with Cassette, REF 5C5479
    Category
    Medical Device
    Distribution
    Distributed nationwide