The Recall Desk

State

Idaho product recalls

20,324 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.

14151–14175 of 20324

  • HighFDA (Devices)·Z-1120-2023·2023-02-22

    Medline Surgical Convenience Kits Recalled for Sterility Compromise

    Medline Industries is recalling 981 surgical convenience kits nationwide because the perforated outer bag does not maintain sterile conditions. Only the kit contents remain sterile, not the exterior wrapping.

    Product
    Surgical convenience kits labeled as: a) MEDLINE PERF. ASSOC. CUT DOWN TRAY, Reorder Number BM17BAD; b) MEDLINE ARM/MINOR DRAPE CSTM, Reorder Number DYNJCD0063
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0286-2023·2023-02-22

    Daptomycin Antibiotic Injectable Syringes Recalled for Lack of Sterility Assurance

    Sentara Infusion Services is recalling Daptomycin pre-filled syringes distributed nationwide due to lack of sterility assurance. Patients using this antibiotic should contact their healthcare provider immediately.

    Product
    DAPTOMYCIN (a)360MG in NS 18ML syringe (b)580MG IN NS 29ML syringe(c) 630MG IN NS 31.5ML used with a home pump; antibiotic, Rx only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1109-2023·2023-02-22

    Surgical convenience kits recalled for compromised sterility packaging

    MEDLINE PAIN TRAY surgical convenience kits (120 units, Lot #22EBA798) are recalled nationwide because a perforated outer bag compromises the sterile barrier. Only the contents inside the kit's inner wrapping remain sterile.

    Product
    Surgical convenience kits labeled as: MEDLINE PAIN TRAY, Reorder Number DYNJRA1122A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0319-2023·2023-02-22

    FDA Class II: TPN solution bags lack sterility assurance

    Sentara Infusion Services is recalling 111 bags of TPN (Total Parenteral Nutrition) solution due to lack of sterility assurance. Products were dispensed nationwide to patients.

    Product
    TPN 107gm/AA, 200gm/DEX, 50gm/LIP 2250mL, (b) 108GM/AA, 330GM/DEX 3000ML, (c) 108GM/AA, 330GM/DEX, 60GM/LIP 3000ML, (d) 37GM/AA, 160GM/DEX 1450ML, (e) 37GM/AA, 160GM/DEX, 25GM/LIP 1450ML, (f) 74-100GM OF PROTEIN B4197 74 Gm, (g) 75GM/AA, 200GM/DEX, 43GM/LIP 2500ML, (h) 90GM/AA ;
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0320-2023·2023-02-22

    TPN parenteral nutrition bags recalled due to lack of sterility

    Sentara Infusion Services is recalling 31 TPN bags due to lack of sterility assurance. The recalled bags with Beyond Use Dates December 24–31, 2022, were dispensed nationwide to patients.

    Product
    TPN (a) 115GM/AA, 215GM/DEX, 25GM/LIP 1150ML, (b)90GM/AA, 215GM/DEX, 25GM/LIP 1150ML, (c) TPN AA: 100GM DEX: 105GM 2700ML, (d) TPN AA: 100GM DEX: 105GM LIP: 45GM 2700ML, (e) TPN: AA100GM ; DEX185GM ; LIP50GM IN 1500ML, (f) TPN: AA 150GM ; DEX 220GM ; LIP 45GM IN 2400 ml, (g) TPN
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0300-2023·2023-02-22

    Lactated Ringers IV Solution Recalled for Sterility Assurance Failure

    Sentara Infusion Services is recalling Lactated Ringers IV solutions (NDC 00338-0117-03) due to lack of sterility assurance. The recall affects 25 bags dispensed nationwide with a Beyond Use Date of December 24-31, 2022.

    Product
    Lactated Ringers packaged in volume of 1000ML, 2500ML, 3000 ML, 3600 ML, 500ML (NDC 00338-0117-03)hydration, Rx Only, use with Curlin pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0270-2023·2023-02-22

    New & Improved Blue Gel Anesthetic Recalled Nationwide for API Discoloration

    HTO Nevada, Inc. is recalling 4,709 bottles of New & Improved Blue Gel Anesthetic nationwide due to discoloration of the epinephrine active pharmaceutical ingredient resulting from a cGMP deviation in the raw material supply.

    Product
    New & Improved Blue Gel Anesthetic, to reduce pain and swelling during pain sensitive procedures, 1 oz bottle, distributed by Dermal Source, Portland, OR, www.dermalsource.com 1-888-568-3223. NDC Code: 80069-008-01. Drug Facts- For use by licensed professionals only, Active Ingre
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0283-2023·2023-02-22

    Ceftriaxone injectable antibiotic recalled for lack of sterility assurance

    Sentara Infusion Services recalled 72 bags of ceftriaxone injectable antibiotic due to lack of sterility assurance. The affected product was distributed nationwide with a beyond-use date of December 24–31, 2022.

    Product
    CEFTRIAXONE (a) 2GM in NS 100ml, (b) 4GM IN NS 200ML, Antibiotic, used with a Curlin or Home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0292-2023·2023-02-22

    Ethanol 70% Syringes Recalled Due to Lack of Sterility Assurance

    Sentara Infusion Services is recalling 17 units of ETHANOL 70% 0.5ML syringes distributed nationwide due to lack of sterility assurance. The syringes may not meet required sterility standards for safe injection.

    Product
    ETHANOL 70% 0.5ML SYRINGE, Cathcare, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1122-2023·2023-02-22

    Medline Surgical Shoulder Suspension Kits Recalled for Sterility Compromise

    Medline is recalling 1,280 SHOULDER SUSPENSION surgical kits nationwide due to a defective perforated bag that fails to maintain sterility on the kit's exterior, potentially compromising the sterile contents inside.

    Product
    Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF, Reorder Number DYNJSHOULDER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0284-2023·2023-02-22

    FDA Recalls D5 NS Injectable Solution for Lack of Sterility Assurance

    Sentara Infusion Services is recalling D5 NS 2300mL, an injectable dextrose-saline solution, due to lack of sterility assurance. The product was dispensed to patients nationwide.

    Product
    D5 NS 2300ML, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0288-2023·2023-02-22

    Dextrose 10% TPN Solution Recalled Due to Sterility Assurance Concerns

    Sentara Infusion Services is recalling Dextrose 10% 720ML TPN injectable solutions nationwide due to lack of sterility assurance. Patients using this product should contact their healthcare provider.

    Product
    Dextrose 10% 720ML, TPN, Rx only, use with a home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0276-2023·2023-02-22

    Ampicillin/Sulbactam antibiotic injection recalled due to sterility concerns

    Sentara Infusion Services is recalling Ampicillin/Sulbactam 3GM intravenous bags due to lack of sterility assurance. The affected product was dispensed nationwide to home infusion patients.

    Product
    Ampicillin/Sulbactam 3GM IN NS 100ML, antibiotic, Rx only, used with a home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0326-2023·2023-02-22

    FDA Recalls Humatrix Microclysmic Gel for Manufacturing Practice Violations

    Consolidated Chemical, Inc. is recalling 3186 bottles of Humatrix Microclysmic Gel nationwide due to deviations from proper manufacturing practices.

    Product
    Humatrix Microclysmic Gel, 8 oz per bottle, Care-Tech Laboratories, Inc., Saint Louis, Missouri 63139.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1127-2023·2023-02-22

    Surgical Circumcision Kits Recalled Due to Non-Sterile Outer Wrapping

    MEDLINE INDUSTRIES is recalling CENTURION MEDICAL PRODUCTS Circumcision Tray kits (Lot 22HMH649) because the outer packaging is non-sterile, though the surgical contents inside remain sterile.

    Product
    Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS CIRCUMCISION TRAY, Reorder Number CIT3345
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1131-2023·2023-02-22

    HydroPICC Catheters Recalled for Incorrect Expiration Date Labeling

    Access Vascular, Inc is recalling HydroPICC 4Fr Single Lumen catheters (Model 80001001) due to incorrect expiration date labeling. The devices expire earlier than the labeled date.

    Product
    HydroPICC 4Fr Single Lumen, 130cm Guidewire - Basic Kit, Model Number 80001001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0325-2023·2023-02-22

    FDA recalls Techni-Care Chloroxylenol antiseptic due to manufacturing deviations

    Consolidated Chemical is recalling Techni-Care Chloroxylenol 3% in 4 oz and 8 oz bottles nationwide due to manufacturing practice violations. No illnesses have been reported.

    Product
    Techni-Care Chloroxylenold 3%, [4 fl oz /118 mL or 8 fl oz/236 mL] per bottle, Care-Tech Laboratories, Inc., Saint Louis, Missouri 63139. NDC 4 oz bottle: 46706-222-01; NDC 8 oz: 46706-222-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·23126·2023-02-16

    Paradise Grills First Generation Outdoor Kitchens Recalled for Fire and Burn Hazards

    About 18,000 Paradise Grills First Generation Outdoor Kitchens are recalled because liquid propane gas can accumulate in the closed lid and cabinets, causing an explosion and severe burns when the grill is relit. Two reports of explosions causing severe burns have been received.

    Product
    Paradise Grills First Generation Outdoor Kitchens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23121·2023-02-16

    Children's Nightgowns Recalled for Flammability Standard Violation

    The Oaks Apparel Company is recalling about 320 children's nightgowns that fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop using them immediately.

    Product
    Children's nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23120·2023-02-16

    Wicked Lights ScanPro Night Hunting Headlamps Recalled for Burn Hazard

    AllPredatorCalls.com is recalling approximately 12,000 Wicked Lights ScanPro night hunting headlamps because a wire short can cause the wire to heat up and melt, posing a burn hazard. The company has received 14 reports of wire heating and melting, including two burn injuries.

    Product
    Wicked Lights ScanPro Night Hunting Headlamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23125·2023-02-16

    KLIM Backcountry Probes A300 Recalled Due to Failure Risk

    KLIM Backcountry Probes A300 can fail to operate when deployed to locate avalanche victims, posing a risk of severe injury or death. Consumers should stop using the product immediately and contact KLIM for a full refund.

    Product
    KLIM Backcountry Probes A300
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23123·2023-02-16

    Children's Nightgowns Recalled for Flammability Standard Violation

    Betsy & Lace children's nightgowns fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 90,550 units sold online from March 2018 through September 2022.

    Product
    Children's nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23127·2023-02-16

    Kids Preferred Disney Character Figurines Recalled for Choking Hazard

    Kids Preferred is recalling soft vinyl Disney character figurines because the arms or legs can detach, posing a choking hazard to children. About 16,140 units were sold nationwide through retailers including BuyBuy Baby and Amazon from May through December 2022.

    Product
    My First Mickey Mouse, Minnie Mouse, Buzz Lightyear, and Stitch Figurines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23122·2023-02-16

    Hatley USA Children's Pajamas and Headbands Recalled

    Hatley USA is recalling about 7,640 children's pajamas and about 300 headbands. The pajamas fail to meet federal flammability standards and pose a burn hazard; the headbands contain excess lead that is toxic if ingested.

    Product
    Children's pajamas and headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23727·2023-02-16

    Linus Bike Recalls Electric Bicycles Due to Crash Hazard

    Linus Bike is recalling about 430 electric bicycles (Cesta 500 and Ero 500 models) because the front fork can crack, posing a crash hazard. No injuries have been reported.

    Product
    Electric bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide