The Recall Desk

State

Idaho product recalls

20,187 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho specifically in their distribution scope.

About recalls in Idaho

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 Idaho 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.

8676–8700 of 20187

  • HighFDA (Devices)·Z-2146-2024·2024-06-26

    PDS II Polydioxanone Sutures Recalled Due to Compromised Sterility

    Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.

    Product
    PDS II (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture and extended wo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0561-2024·2024-06-26

    Teva Recalls Amoxicillin-Clavulanate Antibiotic Tablets Due to Subpotency

    Teva Pharmaceuticals is recalling 34,448 bottles of Amoxicillin and Clavulanate Potassium Tablets USP (Chewable 400mg/57mg) distributed nationwide due to subpotency. The recall is voluntary and initiated by the firm.

    Product
    Amoxicillin and Clavulanate Potassium Tablets USP, Chewable 400mg/57mg, 20-count bottles, Rx only, Manufactured in Canada By: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0093-2272-34
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0562-2024·2024-06-26

    Prescription Drug Duloxetine Recalled for Nitrosamine Impurity Exceeding FDA Limits

    Breckenridge Pharmaceutical recalls Duloxetine 60mg capsules nationwide due to N-nitroso-duloxetine impurity levels exceeding FDA interim limits. Affected lots had current good manufacturing practice (CGMP) deviations.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2161-2024·2024-06-26

    Xstar Safety Slit Knife Recalled for Incorrect Blade Bevel Orientation

    Beaver Visitec International is recalling the Xstar Safety Slit Knife Model 378227 because some units have the blade bevel installed incorrectly—facing downward instead of the intended upward orientation.

    Product
    Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2024·2024-06-26

    PDS Plus Antibacterial Surgical Sutures Recalled for Compromised Sterility

    Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.

    Product
    PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2152-2024·2024-06-26

    Storage Case Design Flaw May Allow Reuse of Single-Use Surgical Instruments

    Howmedica Osteonics Corp. is recalling HRIS Storage & Sterilization Cases (Part 6210-9-900) due to a design flaw that may allow reuse and resterilization of single-use, sterile instruments. This poses a contamination and infection risk.

    Product
    HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2145-2024·2024-06-26

    FDA Recalls VICRYL Plus Antibacterial Sutures Due to Packaging Defect

    Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.

    Product
    VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H VCPB94
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2024·2024-06-26

    Xstar Safety Slit Knife Recalled for Incorrect Blade Configuration

    Beaver Visitec International is recalling 126 Xstar Safety Slit Knives with incorrect blade configuration. The recalled knives have the bevel oriented to the back instead of the front.

    Product
    Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2148-2024·2024-06-26

    MONOCRYL Surgical Sutures Recalled for Packaging Sterility Defect

    Ethicon recalls 306,000 MONOCRYL surgical sutures worldwide due to holes in primary packaging from a manufacturing defect that compromises sterility and could result in infection.

    Product
    MONOCRYL (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated PRODUCT CODE: Y315H Y345H Y359H Y398H Y416H Y417H Y426H Y427H Y935H Y936H Y945H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0555-2024·2024-06-26

    FDA Recalls Dexamethasone Sodium Phosphate Injection Due to Impurity Specification Failure

    Eugia US LLC recalls 70,125 vials of Dexamethasone Sodium Phosphate injection due to failed impurity specifications. Testing found sulfonic acid adduct of dexamethasone phosphate exceeded allowed limits.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0559-2024·2024-06-26

    Cefixime Oral Suspension Recalled for Failed Content Uniformity Specifications

    Lupin Pharmaceuticals is recalling one lot of Cefixime oral suspension (200 mg/5 mL) due to failed content uniformity specifications. The recall affects 3,552 bottles distributed nationwide.

    Product
    CEFIXIME — CEFIXIME (CEFIXIME)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2154-2024·2024-06-26

    Bard Foley Catheter Trays Recalled for Temperature Display Malfunction

    C.R. Bard Inc is recalling 6,420 Foley catheter trays nationwide because some devices may not display temperature readings or may display erratic readings. The malfunction could affect patient monitoring.

    Product
    Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection Control Temperature-Sensing Foley Catheter Tray with Bard Hydrogel and Bacti-Guard Silver Alloy Coating, 350 ml Urine Meter, 16 Fr, Catalog #319416AM. Intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2144-2024·2024-06-26

    VICRYL Sutures recalled due to packaging defect compromising sterility

    Ethicon recalls 341,532 units of VICRYL surgical sutures worldwide due to holes in primary packaging that compromise sterility and could result in infection.

    Product
    VICRYL (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological tissues. PRODUCT CODE: J214H J218H J258H J268H J269H J327H J344H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2153-2024·2024-06-26

    Howmedica Gray Revision Instrument Tray Recalled for Design Enabling Instrument Reuse

    Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.

    Product
    Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0556-2024·2024-06-26

    Drug Recall: Eptifibatide Injection Due to Failed Degradation Specifications

    Eugia US LLC is recalling 15,500 vials of Eptifibatide injection nationwide due to failed impurities and degradation specifications. The defect involves a related substance identified as Eptifibatide dimer.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·24281·2024-06-25

    MGA Entertainment Recalls Miniverse Make It Mini Sets with Liquid Resins

    MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.

    Product
    Miniverse Make It Mini Sets with Liquid Resins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24271·2024-06-20

    myCharge POWER HUB Portable Chargers Recalled for Fire and Burn Hazards

    myCharge is recalling about 567,000 POWER HUB All-In-One 10,000mAh portable chargers sold exclusively at Costco from January 2022 through November 2023 because they can overheat while charging, posing fire and burn hazards. Two residential fires and property damage totaling approximately $165,000 have been reported.

    Product
    myCharge POWER HUB All-In-One 10,000mAh portable chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24273·2024-06-20

    Frontgate Newport Chaise Lounge Chairs Recalled for Finger Crushing and Amputation

    Cinmar recalls approximately 70,000 Frontgate Resort Collection Newport aluminum and teak chaise lounge chairs because the adjustable backrest can descend with force while seated, causing finger crushing and amputation injuries.

    Product
    Frontgate Resort Collection Newport Aluminum and Teak Chaises
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24272·2024-06-20

    JoyJolt Declan Glass Coffee Mugs Recalled for Burn and Laceration Hazards

    MM Products is recalling about 580,000 JoyJolt Declan single-wall glass coffee mugs because they can break and crack when filled with hot liquids, posing burn and laceration hazards. The mugs were sold online from September 2019 through May 2022.

    Product
    JoyJolt Drinkware Declan Single-Wall Glass Coffee Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24276·2024-06-20

    Vitamix Blending Containers and Blade Bases Recalled for Laceration Hazard

    Vitamix Ascent and Venturist Series 8-ounce and 20-ounce blending containers and blade bases can separate from their bases, exposing sharp blades. The company has received 27 reports of lacerations, including 11 from a previous 2018 recall.

    Product
    Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade Bases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24274·2024-06-20

    Theefun Kids Gardening Tools Sets Recalled for Excess Phthalates

    Theefun Kids Gardening Tools Sets (model HJL-001) are recalled because the brown handle strings contain phthalates that exceed federal safety limits. Phthalates are toxic if ingested by young children.

    Product
    Theefun Kids Gardening Tools Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24270·2024-06-20

    Yeti Link Expansion Modules and EC8 Cables Recalled for Fire and Burn Hazards

    Goal Zero is recalling about 34,460 Yeti Link Expansion Modules and EC8 Cables because the connections can overheat and melt, posing fire and burn hazards. Two reports of cables melting inside vehicles have been received with minor property damage but no injuries.

    Product
    Yeti Link Expansion Modules and EC8 Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24275·2024-06-20

    Babboe Cargo Bicycles Recalled for Frame Cracking and Fall Hazard

    Babboe cargo bicycles manufactured by Babboe B.V. are being recalled because their frames can crack, bend, and break, posing a fall hazard to riders. The recall affects about 300 units sold in the United States through bicycle retailers nationwide between January 2011 and March 2024.

    Product
    Cargo bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24279·2024-06-20

    Cedona Natural View Six-Drawer Dressers Recalled for Tip-Over Hazard

    Global Homes USA is recalling about 400 Cedona Natural View six-drawer dressers sold at Rooms To Go for tip-over and entrapment hazards that can injure or kill children if not anchored to a wall.

    Product
    Cedona Natural View six-drawer dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24278·2024-06-20

    Orly Lavender Scented Candles Recalled for Fire and Burn Hazards

    CBOCS Distribution Inc. is recalling about 3,600 lavender scented candles in wooden bread bowls sold at Cracker Barrel Old Country Store from November 2023 through May 2024. The candle flames can reach excessive heights and ignite the wooden bowl, posing fire and burn risks.

    Product
    Lavender scented candles in a round wooden bread bowl
    Category
    Consumer Product
    Distribution
    Distributed nationwide