The Recall Desk

State

Massachusetts product recalls

20,364 recalls have nationwide distribution and so reach Massachusetts. 0 additional recalls listed Massachusetts specifically in their distribution scope.

About recalls in Massachusetts

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 Massachusetts 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.

14026–14050 of 20364

  • HighFDA (Devices)·Z-1177-2023·2023-03-08

    Surgidac Uncoated Braided Polyester sutures recalled due to sterile barrier breach

    Covidien is recalling Surgidac Uncoated Braided Polyester sutures (5-0, 45cm) due to a sterile barrier breach in the breather pouch. This breach may cause infection or vision loss in ophthalmic patients undergoing direct surgical contact.

    Product
    Surgidac Uncoated Braided Polyester suture Product Description D-1764K SURGIDAC* 5-0 WHI 45CM SS24DA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0356-2023·2023-03-08

    Norepinephrine Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 443,483 bottles of Norepinephrine Bitartrate injection nationwide due to lack of sterility assurance in the product.

    Product
    Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 8 mg/250 mL (32 mcg/mL*), 250 mL Single-Dose Container, packaged in 15 x 1 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-316-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1188-2023·2023-03-08

    Maquet CARDIOHELP System extracorporeal support device components recalled for sterility

    Maquet is recalling CARDIOHELP System components due to insufficient evidence of packaging sterility. Non-sterile medical devices could expose patients to infection, sepsis, or ischemia.

    Product
    BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code 70106.9077, BEQ-HLS 7050 USA; HLS Set Advanced 7.0, Product Code 70106.9078. Part of the CARDIOHELP System, a pre-connected set used for extracorporeal respiratory and/or cardiovascular support.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0363-2023·2023-03-08

    Fentanyl Injection Syringes Recalled for Subpotent Active Ingredient

    SCA Pharmaceuticals is recalling 2,125 fentanyl injection syringes nationwide due to subpotency—the product contains less active ingredient than labeled. The firm voluntarily initiated this Class III recall in February 2023.

    Product
    Fentanyl 1,500 mcg/30 mL syringe, Injection for Intravenous Use, Concentration = 50 mcg/mL, Preservative Free, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor CT 06095, NDC# 70004-0200-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0352-2023·2023-03-08

    Microcrystalline Cellulose Pharmaceutical Excipient Recalled for Specification Failure

    DuPont Nutrition USA is recalling BD-102 NF Microcrystalline Cellulose, a pharmaceutical excipient, due to failed conductivity specifications. Affected batches were distributed nationwide and internationally for use in drug manufacturing.

    Product
    BD-102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp., Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copenhagen,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0350-2023·2023-03-08

    DuPont Avicel PH-102 Microcrystalline Cellulose Recalled for Conductivity Specification Failure

    DuPont Nutrition USA is recalling Avicel PH-102 NF microcrystalline cellulose excipient due to failed conductivity specifications indicating potential impurities. The product was distributed nationwide and internationally.

    Product
    Avicel PH- 102 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Cope
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0354-2023·2023-03-08

    Gabapentin 600 mg Tablets Recalled Due to Dosage Strength Mix-Up

    Sciegen Pharmaceuticals is recalling 4,392 bottles of Gabapentin 600 mg tablets after a pharmacist discovered some 800 mg tablets mixed into bottles.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0349-2023·2023-03-08

    Microcrystalline Cellulose Ingredient Recalled Over Failed Impurity Specifications

    DuPont Nutrition USA, Inc. is recalling certain batches of Avicel PH-101 microcrystalline cellulose because it failed quality testing for impurities and degradation. The ingredient showed out-of-specification conductivity levels.

    Product
    Avicel PH- 101 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp. Net Content/Gross Weight 50.0 KG / 54.5 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Cope
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0353-2023·2023-03-08

    Prescription Levothyroxine Sodium Tablets Recalled Due to Sub-Potency

    Alvogen is recalling 21,276 bottles of Levothyroxine Sodium Tablets (Lot HE02221, expiration 05/2023) distributed nationwide and in Puerto Rico due to sub-potency.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0351-2023·2023-03-08

    Avicel PH-200 pharmaceutical excipient recalled for failed conductivity specification

    DuPont is recalling Avicel PH-200, a pharmaceutical excipient, because test results showed conductivity out of specification. No illnesses or injuries have been reported.

    Product
    Avicel PH-200 NF, Microcrystalline Cellulose, NF, Ph. Eur., Jp, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA. Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1, Copen
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V507000·2023-03-07

    Arcimoto hybrid electric vehicles high voltage connector latch defect

    Arcimoto is recalling certain 2019-2022 model year hybrid electric vehicles with a high voltage connector defect that may detach, causing sudden loss of power steering and drive power.

    Product
    ARCIMOTO — 2022 ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V571000·2023-03-07

    Newmar Recreational Vehicles Recalled for Window Adhesive Failure

    Newmar is recalling select 2018-2021 recreational vehicles due to potential window adhesive failure. The vent portion of affected windows may detach, increasing crash and injury risk.

    Product
    NEWMAR — 2020 NEWMAR DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V466000·2023-03-07

    Polaris Slingshot Rearview Camera May Freeze, Affecting Visibility

    Polaris is recalling certain Slingshot models because the rearview camera image may freeze or display a blank screen after shifting into reverse. This defect reduces rear visibility and increases the risk of a crash.

    Product
    POLARIS — 2021 POLARIS SLINGSHOT R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V425000·2023-03-06

    Transmission Actuator Defect in Kenworth and Peterbilt Commercial Trucks

    PACCAR is recalling certain Kenworth and Peterbilt commercial trucks due to transmission actuator defects that may cause unexpected gear shifts, increasing crash risk. Affected owners should contact dealers for free replacement.

    Product
    KENWORTH — 2022 KENWORTH T180
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V424000·2023-03-06

    2022 Kenworth T180 ABS warning light malfunction recall

    PACCAR is recalling certain 2022 Kenworth T180 and 2023 Kenworth T280 and Peterbilt 535 vehicles because the ABS warning light may not illuminate during an ABS malfunction, potentially increasing crash risk. Dealers will provide a free software update.

    Product
    KENWORTH — 2022 KENWORTH T180
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V402000·2023-03-05

    2021 INFINITI QX50 Steering Knuckle Structural Defect - Multiple Models Affected

    Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.

    Product
    INFINITI — 2021 INFINITI QX50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V398000·2023-03-05

    RAM 3500, 4500, and 5500 vehicles recalled for wheel stud failure

    Chrysler is recalling RAM trucks because incorrect manual torque specifications can cause wheel studs to over-tighten, break, and lead to wheel separation and possible crashes.

    Product
    RAM — 2013 RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V311000·2023-03-05

    2022 Winnebago Micro Minnie Solar Panel Fasteners May Loosen Causing Detachment

    Winnebago is recalling 2022 Micro Minnie travel trailers due to loose solar panel mounting hardware that may cause the solar panel to detach. A detached panel can become a road hazard and increase crash risk.

    Product
    WINNEBAGO — 2022 WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V312000·2023-03-05

    Volkswagen ID.4 Door Handles May Open Unexpectedly Due to Water Intrusion

    Certain 2021-2022 Volkswagen ID.4 vehicles have door handles that may allow water to enter the circuit board assembly, potentially causing doors to open unexpectedly while driving. Volkswagen will update vehicle software and inspect door handles at no cost to owners.

    Product
    VOLKSWAGEN — 2021 VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V313000·2023-03-05

    2022 Porsche 911 Carrera recalled for missing body welds

    Porsche is recalling certain 2022 911 Carrera and related models due to missing welds in the vehicle body from a production process error. Missing welds could reduce crash protection and increase the risk of injury.

    Product
    PORSCHE — 2022 PORSCHE 911 CARRERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V262000·2023-03-04

    2019-2021 Autocar Xpeditor Vehicles Recall: Inoperable Hazard Lights

    Autocar is recalling 2019-2021 Xpeditor vehicles because the hazard lights do not function when the ignition is off, increasing crash risk. Dealers will repair or replace the wire harness at no charge.

    Product
    AUTOCAR — 2019 AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V261000·2023-03-04

    2021 Mercedes-Benz AMG GLC63 S Headlight Failure Recall

    Mercedes-Benz is recalling certain 2021 GLC models because the headlight electrical connection may not be watertight, risking headlight failure. Reduced visibility increases crash risk.

    Product
    MERCEDES-BENZ — 2021 MERCEDES-BENZ AMG GLC63 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V157000·2023-03-03

    2022 Winnebago travel trailers recalled for improperly welded couplers

    Winnebago is recalling certain 2022 Micro Minnie, Minnie, and Voyage travel trailers because the coupler was improperly welded, which may cause the trailer to separate from the tow vehicle and increase crash risk.

    Product
    WINNEBAGO — 2022 WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V143000·2023-03-03

    2023 Mack Granite Trucks Recalled for Loose Axle Fasteners

    Mack is recalling approximately 17 model-year 2023 Granite trucks because front-drive steer axle fasteners may not have been properly tightened and could come loose, risking loss of steering control and crashes.

    Product
    MACK — 2023 MACK GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V142000·2023-03-03

    2023 Toyota Tundra Hybrid Tonneau Cover May Detach While Driving

    Toyota is recalling 2022-2023 Tundra and Tundra Hybrid trucks with Toyota genuine tonneau covers. The cover's attachment joints may loosen and allow the cover to detach while driving, creating a road hazard.

    Product
    TOYOTA — 2023 TOYOTA TUNDRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide