The Recall Desk

State

New Hampshire product recalls

73,495 recalls have nationwide distribution and so reach New Hampshire. 4,474 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,474
Critical
606
Severe
1,044
Most recent
2026-10-14

Of the 4,474 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,044 (23%) are Severe.

These figures cover only the 4,474 recalls whose distribution notice names New Hampshire specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23451–23475 of 77969

  • HighFDA (Devices)·Z-0369-2022·2021-12-22

    Cardinal Health Surgical Gowns Recalled for Potential Packaging Seal Defects

    Cardinal Health is recalling 169,262 SmartSleeve surgical gowns due to potential package seal defects that could compromise sterility. Multiple affected lot numbers span 2020-2021 production with worldwide distribution.

    Product
    SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-Large SKU: 9011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0386-2022·2021-12-22

    Activforce 2 force measurement device recalled for inaccurate measurement

    Activforce 2 medical devices (145 units) are being recalled due to a manufacturing defect causing inaccurate force measurement, which may lead to incorrect treatment planning. Verify your device's serial number against the FDA recall list.

    Product
    activforce 2 package labeling: Model: Activ5-M R 201-200563
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Devices)·Z-0377-2022·2021-12-22

    Cardinal Health RoyalSilk Surgical Gowns Recalled for Potential Sterility Compromise

    Cardinal Health has recalled RoyalSilk Non-Reinforced Surgical Gowns XX-large due to the potential for packaging seals to open, which could compromise product sterility. The recall affects approximately 9,990 units distributed worldwide.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns XX-large SKU: 9578
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0376-2022·2021-12-22

    RoyalSilk Surgical Gowns Recalled for Potential Sterility Compromise

    Cardinal Health is recalling 270,839 units of RoyalSilk Non-Reinforced Surgical Gowns (X-large, SKU 9548) due to potential packaging seal failures that could compromise sterility.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns X-large SKU: 9548
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0385-2022·2021-12-22

    Activ5 Smart Fitness Device Recalled for Inaccurate Force Measurement

    Activbody is recalling the Activ5 smart fitness device due to manufacturing defects causing inaccurate force measurements, which may lead to incorrect treatment planning. The device was distributed nationwide.

    Product
    Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5, the first isometrics-based smart strength training and rehabilitation device.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Devices)·Z-0358-2022·2021-12-22

    EVLP Convenience Pack Recalled for Expired Injectable Component

    Medline Industries is recalling EVLP Convenience Pack/Kit due to a NaCl injectable component that expired in April 2020, despite the kit's label showing a later expiration date. Users may unknowingly use expired medication.

    Product
    EVLP Convenience Pack/Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0331-2022·2021-12-22

    Tang Orange Drink Mix Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Tang orange drink mix powder (2.2 kg) due to potential glass and metal contamination. The product was distributed nationwide and internationally.

    Product
    Tang orange drink mix powder 2.2 KG UPC 66188057502
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0326-2022·2021-12-22

    Arizona Arnold Palmer Drink Mix Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Arizona Arnold Palmer Half Iced Tea & Half Lemonade drink mix powder (73 oz) because the product may contain glass and metal fragments.

    Product
    Arizona Arnold Palmer Half Iced Tea & Half Lemonade drink mix powder 73 oz. UPC 043000086643
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0370-2022·2021-12-22

    Surgical Gowns Recalled Due to Potential Packaging Seal Defects

    Cardinal Health is recalling SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns (X-Large, SKU 9041) due to potential open packaging seals that could compromise sterility. The recall affects 231,219 units distributed worldwide.

    Product
    SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-X-Large SKU: 9041
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0279-2022·2021-12-22

    Lidocaine Hydrochloride Topical Solution Recalled for Superpotency

    Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution USP 4% due to manufacturing deviations. The recalled lot was produced at a facility where cracked seals in caps led to superpotent products.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0281-2022·2021-12-22

    Lidocaine Hydrochloride Topical Solution recalled for CGMP deviations

    Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution USP 4% due to manufacturing deviations. Affected lots were made at a facility where cracked seals in caps were found on related products.

    Product
    Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena, NJ 08310, NDC 52565-009-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0285-2022·2021-12-22

    Telmisartan and Hydrochlorothiazide Tablets Recalled for Superpotency

    Torrent Pharma Inc. is recalling Telmisartan and Hydrochlorothiazide Tablets USP 40 mg/12.5 mg due to superpotency. The affected batch (BZ74G001, expiring 12/2021) contains approximately 27,312 bottles distributed nationwide.

    Product
    Telmisartan and Hydrochlorothiazide Tablets, USP, 40 mg/12.5 mg, 30 count bottles, Rx only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC: 13668-159-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0282-2022·2021-12-22

    Clindamycin and Benzoyl Peroxide Gel Recalled for Superpotent Formulation

    TOLMAR, Inc. is recalling Clindamycin and Benzoyl Peroxide Gel, 1%/5%, nationwide due to a superpotent (higher-than-intended active ingredient) formulation. The voluntary recall affects three specific lots.

    Product
    Clindamycin and Benzoyl Peroxide Gel, 1%/5% 25 g jars, Rx only, Mfg by TOLMAR Inc. Fort collins, CO 80526, NDC 0781-7263-68
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0329-2022·2021-12-22

    Kool-Aid Strawberry Drink Mix Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Kool-Aid strawberry drink mix powder (19 oz.) due to potential glass and metal contamination. The recall affects approximately 289,221 cases distributed nationally and internationally.

    Product
    Kool-Aid strawberry drink mix powder 19 oz. UPC 043000953556
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0362-2022·2021-12-22

    Bedside PICC CDS Convenience Kit Recalled for Expired Saline Component

    Medline Industries is recalling the Bedside PICC CDS Convenience Kit because a saline injection bag component expired in April 2020 while the kit's expiration date was later. No injuries have been reported.

    Product
    Bedside PICC CDS Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0327-2022·2021-12-22

    Kool-Aid Cherry Drink Mix Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Kool-Aid cherry drink mix powder in multiple sizes due to potential glass and metal contamination. The recall affects 289,221 cases distributed nationwide and internationally.

    Product
    Kool-Aid cherry drink mix powder 19 oz. UPC 043000953532 19 oz. UPC 043000034163 63 oz. UPC 043000082201
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0332-2022·2021-12-22

    Tang Orange Drink Mix Powder Recall for Potential Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Tang orange drink mix powder in three sizes due to potential contamination with glass and metal particles. The affected product was distributed nationwide and internationally.

    Product
    Tang orange drink mix powder 20 oz. UPC 043000032275 58.9 oz. UPC 043000082171 72 oz. UPC 043000032268
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00A000·2021-12-21

    2022 Jeep Wagoneer and Grand Wagoneer Rearview Display Software Defect

    Certain 2022 Jeep Wagoneer and Grand Wagoneer vehicles have a radio software defect that may prevent the rearview camera display from functioning, reducing rear visibility and increasing crash risk. Dealers will reprogram the radio software free of charge.

    Product
    JEEP — JEEP GRAND WAGONEER, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00B000·2021-12-21

    Tesla Model S Hood Latch Misalignment Could Cause Unexpected Hood Opening During Driving

    Tesla is recalling 2014-2021 Model S vehicles due to a misaligned front trunk latch assembly that may prevent the secondary hood latch from engaging. This could allow the hood to open unexpectedly during driving, obstructing the driver's view and increasing crash risk.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V998000·2021-12-20

    Altec Recalls 2017-2021 Aerial Devices Due to Hydraulic Plumbing Defect

    Altec Industries is recalling 2017-2021 aerial devices because incorrect hydraulic plumbing could allow booms to overextend, increasing the risk of tipping and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V996000·2021-12-20

    Crane Carrier Recalls LET2 Trucks Due to Fuel Leak Fire Risk

    Crane Carrier is recalling 2019-2021 LET2 vehicles because fuel tubes may crack, causing a high-pressure leak that increases fire risk.

    Product
    CRANE CARRIER — CRANE CARRIER, CRANE LET2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V995000·2021-12-20

    Van Hool Recalls 2020-2021 Buses Due to Fuel Leak Fire Risk

    Van Hool is recalling 139 CX45, TX45, and TDX25 buses because fuel tubes may crack, causing high-pressure leaks that could lead to fire.

    Product
    VAN HOOL — VAN HOOL CX45, TX45, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V993000·2021-12-20

    Cruiser Recalls 2021-2022 Travel Trailers for Incorrect Tire Labeling

    Cruiser RV is recalling 2021-2022 Shadow Cruiser and 2022 Twilight travel trailers because certification labels may display incorrect tire information, potentially leading to the installation of wrong tires.

    Product
    CRUISER RV — CRUISER RV, CRUISER SHADOW CRUISER, TWILIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide