State

New Hampshire product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51501–51525 of 78316

ModerateFDA (Devices)·Z-1687-2016·2016-05-25
Diamedix IgG Test Kits Recalled Due to Gel-Like Substance in Diluent
Diamedix Corporation is recalling 94 Is-EBV-EA-D and Is-Mumps IgG Test Kits because a gel-like substance was found in the sample diluent, potentially compromising performance.
Product
Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1685-2016·2016-05-25
Diamedix Is-Mumps IgG Test Kit Recalled Due to Sample Diluent Contamination
Diamedix Corporation is recalling 697 Is-Mumps IgG Test Kits because a gel-like substance was found in the sample diluent, which could compromise product performance.
Product
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1686-2016·2016-05-25
Diamedix IgG Test Kits Recalled Due to Sample Diluent Contamination
Diamedix Corporation is recalling 588 EBV-VCA and Mumps IgG test kits because a gel-like substance in the sample diluent could compromise performance.
Product
Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1674-2016·2016-05-25
Zimmer 2.7 mm Cortical Screws Recalled for Potential Tray Hole
Zimmer Manufacturing B.V. is recalling specific lots of 2.7 mm Cortical Screws because a small hole may be present in the inner tray of the sterile packaging.
Product
Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping, 14 mm Length 47482701401
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1351-2016·2016-05-25
Bunge Vegetable Oil Recalled for Foreign Material in Jugs
Bunge Oil North America Inc. is recalling EB Golden Fry Clear Liquid Shortening due to the presence of foreign material inside the jugs.
Product
EB Golden Fry Clear Liquid Shortening, 35 lbs. (15.88 kg), Distributed By: EB Express Provisions, Inc., 181-191 Vanderpool Street, Newark, NJ 07114, UPC 0 00 78684 73630 0
Category
Food
Distribution
9 states
ModerateFDA (Devices)·Z-1683-2016·2016-05-25
Zimmer Manufacturing Recalls Hip and Trauma Implant Screws Due to Tray Defect
Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.
Product
Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp ii acetabular cup bone screw selftap 6.5x20mm 00662406520 Hgp ii acetabular cup bone screw selftap 6.5x25mm 00662406525 Hgp ii acetabular cup bone screw selftap 6.5x35mm 00662406535 Hgp ii acetabular cup bone…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1337-2016·2016-05-25
Bunge Canola Deep Frying Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling specific lots of Nutra-Clear NT Ultra Canola Deep Frying Oil due to the presence of foreign material inside the jugs.
Product
Nutra-Clear NT Ultra - Bunge Canola Deep Frying Oil (High Stability), 35 lb., (15.88 kg), MFD in USA by: Bunge Oils, St. Louis, MO 63146-1000, UPC 0 00 78684 72477 2
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1353-2016·2016-05-25
Bunge Daily Chef Soybean Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling Daily Chef Food Service Pure Soybean Oil due to the presence of foreign material inside the jugs.
Product
Daily Chef Food Service Pure Soybean Oil (Aceite de Soya), Net/Neto 4.5 Gal (17L) and Net Wt/Peso Neto, 35 lbs. (15.8 kg), Distributed By: Sam's West Inc., Bentonville, AR 72716, UPC 0 78742 06151 1
Category
Food
Distribution
9 states
ModerateFDA (Devices)·Z-1675-2016·2016-05-25
Zimmer Universal Locking System Cortical Screws Recalled for Packaging Defect
Zimmer Manufacturing B.V. is recalling specific lots of sterile hip and trauma implant screws because a small hole may be present in the inner tray.
Product
Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping 18 mm length 47493501801
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1348-2016·2016-05-25
Bunge Smart Source Creamy Soybean Frying Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling 60 cases of Smart Source Creamy Soybean Frying Oil due to the presence of foreign material inside the jugs.
Product
Smart Source Creamy Soybean Frying Oil (Aceite de Soja Cremosa Para Freir), Net Wt./Peso Neto, 35 lbs. (15.88 kg), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, Product of USA/Producto de EE.UU., UPC 0 08 22486 13045 9
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1336-2016·2016-05-25
Bunge Soy Clear Fry Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling 3,240 cases of Bunge Soy Clear Fry Oil OU due to the presence of foreign material inside the jugs.
Product
Bunge Soy Clear Fry Oil OU, 35 lb., Manufactured by: Bunge Oils, Inc. Kearny, NJ 07032, UPC 00078684692026
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1340-2016·2016-05-25
Bunge Harvest Value Canola Salad Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling Harvest Value Canola Salad Oil due to the presence of a foreign material inside the jugs.
Product
Harvest Value Canola Salad Oil, 35 lb., (15.88 kg), Distributed By: U.S. Foodservice, Inc,, Rosemont, IL 60018, UPC 5 07 58108 02454 5
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1360-2016·2016-05-25
Bunge Smart Source Canola Salad Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling 60 cases of Smart Source Canola Salad Oil due to the presence of a foreign material inside the jugs.
Product
Smart Source Canola Salad Oil (Aceite de Canola Para Ensalada), Net Wt./Peso Neto 35 lbs. (15.88 kg), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, UPC 0 08 22486 17655 6
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1343-2016·2016-05-25
Bunge Smart Source Soybean Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling 1,080 cases of Smart Source Clear Soybean Frying Oil due to the presence of a foreign material inside the jugs.
Product
Smart Source Clear Soybean Frying Oil (Aceite de Soya Transparente Para Freir), Net Wt./Peso Neto 35 lbs. (15.88 kg), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, UPC 0 08 22486 13046 6
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1362-2016·2016-05-25
MegaFood Multi for Women 40+ Recalled for Missing Iron Warning
FoodState, Inc. is recalling MegaFood Multi for Women 40+ multivitamin bottles because the labels lack the required iron warning statement and child-resistant cap.
Product
MegaFood Multi for Women 40+, Multivitamin & Mineral Dietary Supplement packaged in glass bottles UPC:5149410321 -Packaged 60 tablets; UPC:5149410322 -Packaged 120 tablets
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1342-2016·2016-05-25
Bunge Vegetable Oil Recalled for Foreign Material Presence
Bunge Oil North America Inc. is recalling Katy's Kitchen Soybean Salad Oil due to the presence of foreign material inside the jugs.
Product
Katy's Kitchen Soybean Salad Oil (Soya Aceite Para Ensalada), Marketed by/Comercializado por Independent Marketing Alliance, Houston, TX 77079, Product of USA/Producto de EE.UU., UPC 0 08 22486 13034 3
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1352-2016·2016-05-25
Bunge Daily Chef Frying Oil Recalled for Foreign Material
Bunge Oil North America Inc. is recalling specific lots of Daily Chef Food Service Pure Clear Frying Oil due to the presence of foreign material inside the jugs.
Product
Daily Chef Food Service Pure Clear Frying Oil (Aceite Transparente Para Freir), Net/Neto 4.5 Gal (17L) and Net Wt/Peso Neto, 35 lbs. (15.8 kg), Distributed By: Sam's West Inc., Bentonville, AR 72716, UPC 0 78742 06148 1
Category
Food
Distribution
9 states
ModerateFDA (Food)·F-1338-2016·2016-05-25
Bunge Canola Oil Recalled for Foreign Material Presence
Bunge Oil North America Inc. is recalling Harvest Value Canola Liquid Frying Oil due to the presence of a foreign material inside the jugs.
Product
Harvest Value Canola Liquid Frying Oil, 35 lb., (15.88 kg), Distributed By: U.S. Foodservice, Inc,, Rosemont, IL 60018, UPC 5 07 58108 01988 6
Category
Food
Distribution
9 states
LowFDA (Drugs)·D-0856-2016·2016-05-25
Allegiant Health Recalls Col-Rite Stool Softeners for Potency Issues
Allegiant Health is recalling specific lots of Col-Rite stool softeners because they failed potency tests. Consumers should stop using the product and return it to the pharmacy.
Product
col-rite (docusate sodium) stool softener softgels, 50 mg, packaged in a) 30-count, item 351104, UPC 0 11822 51104 9; and b) 60-count, item 357392, UPC 0 11822 57392 4; DISTRIBUTED BY: RITE AID, 30 HUNTER LANE, CAMP HILL , PA 17011.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0854-2016·2016-05-25
Hospira Recalls Magnesium Sulfate Injection Due to pH Failures
Hospira Inc. is recalling 715,200 vials of Magnesium Sulfate Injection, USP 50% due to confirmed high out-of-specification pH results.
Product
Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.
Category
Drug
Distribution
Distributed nationwide
CriticalNHTSA·16V352000·2016-05-24
Chrysler Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk
Chrysler is recalling approximately 4.6 million vehicles because passenger air bag inflators may rupture, sending metal fragments into the cabin. Owners are advised not to drive until repairs are complete.
Product
DODGE — DODGE, MITSUBISHI, JEEP DURANGO, RAM 3500, RAIDER, WRANGLER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V347000·2016-05-24
Honda Recalls GL1800 Motorcycles Due to Air Bag Inflator Rupture Risk
Honda is recalling 2006-2010 GL1800 motorcycles in specific regions because air bag inflators may rupture during deployment, potentially causing serious injury or death.
Product
HONDA — HONDA GL1800
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V378000·2016-05-24
Vermeer Recalls BC900XL Wood Chippers Due to Chassis Weld Defect
Vermeer is recalling 2012-2016 BC900XL wood chippers because improper chassis welds could cause the unit to separate from the tow vehicle, increasing crash risk.
Product
VERMEER — VERMEER BC900XL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V349000·2016-05-24
Nissan Recalls Infiniti and Versa Vehicles for Air Bag Inflator Defect
Nissan is recalling specific Infiniti and Nissan Versa vehicles because the passenger air bag inflators may rupture, potentially causing serious injury or death.
Product
INFINITI — INFINITI, NISSAN FX45, FX35, I35, M35
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V348000·2016-05-24
Hyundai Recalls 2016 Tucson Vehicles Due to Hood Latch Defect
Hyundai is recalling 81,000 model year 2016 Tucson vehicles because the secondary hood latch may fail to secure the hood, increasing crash risk.
Product
HYUNDAI — HYUNDAI TUCSON
Category
Vehicle
Distribution
Distributed nationwide