The Recall Desk

State

New Hampshire product recalls

19,713 recalls have nationwide distribution and so reach New Hampshire. 0 additional recalls listed New Hampshire specifically in their distribution scope.

About recalls in New Hampshire

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect New Hampshire consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

851–875 of 19713

  • ModerateFDA (Devices)·Z-1982-2026·2026-05-06

    BD GasPak EZ CO2 Pouch System gas generating sachets underperforming

    Becton Dickinson is recalling certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems because gas generating sachets may produce carbon dioxide levels below specification.

    Product
    BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1969-2026·2026-05-06

    Philips MR 7700 MRE Upgrade MRI Equipment Stiffness Value Error Risk

    Philips is recalling 15 units of its MR 7700 with MR Elastography upgrade due to potential stiffness value errors in MRI scans when specific image reconstruction parameters are used with the Resoundant algorithm.

    Product
    Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0505-2026·2026-05-06

    Fentanyl Citrate Injectable Solution Recalled for cGMP Deviations

    Wells Pharma of Houston LLC has recalled fentanyl citrate injectable solution (1250 mcg/25mL) distributed nationwide due to cGMP deviations. The recall involves 50 syringes from Lot 011226204250063, expiring 05/14/2026.

    Product
    fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pharma of Houston, NDC 73702-204-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1988-2026·2026-05-06

    DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall

    DePuy Synthes is recalling 3 units of ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM due to external sterile packaging adhered to internal packaging, potentially compromising sterility.

    Product
    Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1946-2026·2026-05-06

    Disposable Mixing Bowls with Spatula recalled for compromised sterile barrier

    Zimmer, Inc. is recalling Disposable Mixing Bowls with Spatula (Model 00-5049-011-00) due to package seal defects that may compromise the sterile barrier. Ten complaints have been received identifying incomplete seals, wrinkles, or peeling seals.

    Product
    Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number: 00-5049-011-00 Software Version: N/A Product Description: Mixing Bowl and Spatula Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1962-2026·2026-05-06

    Philips Ingenia Elition S MRI stiffness value error correction

    Philips Ingenia Elition S MRI systems with MR Elastography may display incorrect voxel size settings in the default scan protocol when certain image reconstruction parameters are used, potentially leading to stiffness value errors.

    Product
    Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3. Model Number (REF): 782137.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1968-2026·2026-05-06

    Philips SmartPath to Ingenia Elition X MR Elastography Stiffness Value Errors

    Philips is recalling three models of SmartPath to Ingenia Elition X with MR Elastography devices due to potential stiffness value errors when specific image reconstruction parameters are combined with Resoundant's algorithm.

    Product
    Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model Number (REF): 782163.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1961-2026·2026-05-06

    Philips Ingenia Ambition X MRI Systems Stiffness Value Error Recall

    Philips Ingenia Ambition X MRI systems with MR Elastography may produce incorrect stiffness values due to image reconstruction parameter errors, affecting diagnostic accuracy.

    Product
    Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3. Model Number (REF): 782138. 4. Model Number (REF): 782160.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0494-2026·2026-05-06

    Levocarnitine Injection USP Missing Label Recall

    American Regent, Inc. is recalling Levocarnitine Injection USP (1 g/5 mL) due to missing labeling on certain lots. The affected product was distributed nationwide.

    Product
    LEVOCARNITINE — LEVOCARNITINE (LEVOCARNITINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1997-2026·2026-05-06

    Heraeus PALAMIX uno Dental Material Mixing Rod Loose Risk Recall

    Heraeus Medical is recalling PALAMIX uno dental material because the mixing rod may come loose during mixing in units older than 1.5 years. The shelf life has been reduced from 3 years to 1.5 years.

    Product
    Heraeus, PALAMIX uno. Material Number: 66057893.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0509-2026·2026-05-06

    CVS Lidocaine Wound Gel recalled for failed pH specifications

    CVS Lidocaine Wound Gel is being recalled because it failed pH specifications. The affected product is distributed nationwide.

    Product
    Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1998-2026·2026-05-06

    Heraeus PALAMIX duo dental mixing system batches worldwide recall

    Heraeus Medical is recalling PALAMIX duo dental mixing units (Material Number 66057897) because the mixing rod may come loose from its lock during use in units older than 1.5 years. The shelf life is being reduced from 3 years to 1.5 years.

    Product
    Heraeus, PALAMIX duo. Material Number: 66057897.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V378000·2026-05-05

    [pending] 2023 GRAND DESIGN SOLITUDE

    Pending LLM rewrite. Source: NHTSA 24V378000.

    Product
    GRAND DESIGN — 2023 GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V377000·2026-05-05

    [pending] 2025 LION LIONC

    Pending LLM rewrite. Source: NHTSA 24V377000.

    Product
    LION — 2025 LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V283000·2026-05-05

    [pending] 2021 TESLA MODEL Y

    Pending LLM rewrite. Source: NHTSA 26V283000.

    Product
    TESLA — 2021 TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V254000·2026-05-04

    [pending] 2025 MERCEDES-BENZ G 580

    Pending LLM rewrite. Source: NHTSA 25V254000.

    Product
    MERCEDES-BENZ — 2025 MERCEDES-BENZ G 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V302000·2026-05-04

    [pending] 2021 MINI COOPER SE

    Pending LLM rewrite. Source: NHTSA 24V302000.

    Product
    MINI — 2021 MINI COOPER SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V301000·2026-05-04

    [pending] 2022 NEWMAR BAY STAR

    Pending LLM rewrite. Source: NHTSA 24V301000.

    Product
    NEWMAR — 2022 NEWMAR BAY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V304000·2026-05-04

    [pending] 2024 NISSAN SENTRA

    Pending LLM rewrite. Source: NHTSA 24V304000.

    Product
    NISSAN — 2024 NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V257000·2026-05-04

    [pending] 2022 VOLVO VN

    Pending LLM rewrite. Source: NHTSA 25V257000.

    Product
    VOLVO — 2022 VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V129000·2026-05-03

    [pending] 2025 GMC SIERRA 3500

    Pending LLM rewrite. Source: NHTSA 26V129000.

    Product
    GMC — 2025 GMC SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V128000·2026-05-03

    [pending] 2021 TOYOTA HIGHLANDER

    Pending LLM rewrite. Source: NHTSA 26V128000.

    Product
    TOYOTA — 2021 TOYOTA HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V097000·2026-05-02

    [pending] 2023 THOR MOTOR COACH GEMINI

    Pending LLM rewrite. Source: NHTSA 25V097000.

    Product
    THOR MOTOR COACH — 2023 THOR MOTOR COACH GEMINI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V067000·2026-05-02

    [pending] 2020 JAGUAR I-PACE

    Pending LLM rewrite. Source: NHTSA 26V067000.

    Product
    JAGUAR — 2020 JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V165000·2026-05-02

    [pending] 2024 BMW K 1600 GT

    Pending LLM rewrite. Source: NHTSA 24V165000.

    Product
    BMW — 2024 BMW K 1600 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide