The Recall Desk

State

Mississippi product recalls

20,322 recalls have nationwide distribution and so reach Mississippi. 0 additional recalls listed Mississippi specifically in their distribution scope.

About recalls in Mississippi

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 Mississippi 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.

12226–12250 of 20322

  • HighFDA (Devices)·Z-2329-2023·2023-08-09

    Ultrasound Gel in Medline Procedural Kits Recalled Over Sterility Specification Concerns

    Medline Industries recalled approximately 154,900 Custom Sterile and Non-Sterile Procedural Kits worldwide because the sterile ultrasound gel component may not meet sterility specifications.

    Product
    Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PROBE COVER PACK, Model Number: DYNDA1219
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1078-2023·2023-08-09

    Phenylephrine Injection Syringes Recalled Due to Sterility Validation Failure

    Central Admixture Pharmacy Services Inc. is recalling 16,971 syringes of phenylephrine injection due to lack of validation data for sterilization processes. The product was distributed nationwide.

    Product
    PHENYLephrine in 0.9 sodium chloride, 400 mcg /10 mL, (40 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6007-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2326-2023·2023-08-09

    FDA Recalls Medline Procedural Kits Due to Potential Sterility Failure

    Medline Industries is recalling 22 procedural kits because the included ultrasound gel may not be sterile as labeled. The kits were distributed worldwide.

    Product
    Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. PREMIUM CLOSUREPLUS PACK, Model Number: DYNJ54326A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2299-2023·2023-08-09

    Medline Procedural Kits Recalled for Ultrasound Gel Sterility Defect

    Medline Industries recalls 104,755 procedural kits due to potential sterility defect in ultrasound gel component. No illnesses or injuries have been reported.

    Product
    Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. MULTI-LUMEN CVC BUNDLE KIT, Model Number: ECVC475; b. MULTI-LUMEN CVC INSERTION BUNDLE, Model Number: ECVC3900; c. MULTIMED 16G 1L 20CM CVC STOCK+BUNDLE US, Mode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2331-2023·2023-08-09

    Medline Procedural Kits Recalled Due to Sterility Specification Failure

    Medline Industries recalls 15,945 Custom Sterile and Non-Sterile Procedural Kits due to potential failure of the Turkuaz ultrasound gel component to meet sterility specifications. The kits were distributed worldwide between April 2020 and April 2023.

    Product
    Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. ANGIO, Model Number: DYNJ905151A; b. ANGIO/VENO PACK, Model Number: DYNJ58346A; c. ANGIOGRAPHIC PACK, Model Number: DYNJ57442C, DYNJ64081A; d. ANGIOGRA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1008-2023·2023-08-09

    Neonatal TPN Starter Bags Recalled for Lack of Sterility Assurance

    Central Admixture Pharmacy Services recalls 124 neonatal TPN starter bags nationwide due to lack of sterility assurance from missing decontamination validation data.

    Product
    Neonatal TPN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with CALCIUM and HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0421-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1060-2023·2023-08-09

    HYDROmorphone Injectable Syringes Recalled for Lack of Sterilization Validation

    Central Admixture Pharmacy Services is recalling 5,259 HYDROmorphone injectable syringes nationwide due to lack of validation data for sterilization, raising concerns about product sterility assurance.

    Product
    HYDROmorphone in 0.9% sodium chloride, 30 mg/30 mL, (1 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2012-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1043-2023·2023-08-09

    Fentanyl injection syringes recalled for unvalidated sterilization process

    Central Admixture Pharmacy Services is recalling 5,124 fentanyl syringes because the manufacturer lacks validation that its sterilization process is effective. The nationwide recall affects multiple lot numbers distributed through September 2023.

    Product
    fentaNYL, 1250 mcg/25 mL, (50 mcg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0946-2023·2023-08-09

    Prescription oral drug solution recalled due to manufacturing quality deviation

    The Ritedose Corporation is recalling Cromolyn Sodium Oral Solution (Concentrate) due to a manufacturing deviation. Lot 23CE2, distributed nationwide, was released prior to obtaining required supplier approval.

    Product
    CROMOLYN SODIUM ORAL SOLUTION (CONCENTRATE) — CROMOLYN SODIUM ORAL SOLUTION (CONCENTRATE) (CROMOLYN SODIUM ORAL SOLUTION (CONCENTRATE))
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2251-2023·2023-08-09

    Surgical table drapes and infection control kits recalled for naphthalene odor

    Microtek Medical Inc. is recalling certain lots of surgical table drapes and infection control kits due to detection of naphthalene odor. The affected products are distributed nationwide in the US and in Canada.

    Product
    Equipment and table drapes and Surgical Room Turnover (SRT) Kits: (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile; (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-steril
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2250-2023·2023-08-09

    Ecolab Medical Device Drapes Recalled for Naphthalene Odor

    Microtek Medical Inc. is recalling certain lots of Ecolab sterile medical device drapes due to naphthalene odor. The recall affects five models distributed in the United States and Canada.

    Product
    Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape, 91 cm x 51 cm (36 in x 20 in), Model 63620RT, pkgd. 25/case, sterile; (2) Ecolab Microtek Banded Bag with Elastic Opening, Circular, 102 cm (40 in), Model 60040S, pkgs. 25/case, sterile; (3) Ecolab M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2249-2023·2023-08-09

    Gore Tips Set Device Recall: Incorrect Expiration Date Labeling

    Creganna Medical Devices is recalling three lots of Gore Tips Set Device due to incorrect expiration date labeling. Affected devices may be used past their actual expiration date.

    Product
    Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V512000·2023-08-07

    Alliance RV Paradigm and Valor Travel Trailers Awning Weld Separation

    Alliance RV is recalling 2022-2023 Paradigm and Valor travel trailers due to electric retractable awning weld separation that may allow the awning to drop unexpectedly, increasing injury risk.

    Product
    ALLIANCE RV — 2023 ALLIANCE RV PARADIGM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V514000·2023-08-07

    Volkswagen Atlas Cross Sport Rearview Camera Software Defect Recall

    Volkswagen is recalling certain 2021-2022 Atlas Cross Sport vehicles due to an infotainment system defect that may prevent the rearview camera image from displaying. This loss of rear visibility increases crash risk.

    Product
    VOLKSWAGEN — 2021 VOLKSWAGEN ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V513000·2023-08-07

    2022 BMW X3 Fuel Rail Defect May Cause Engine Fire

    BMW is recalling 2022 X3 xDrive30i vehicles because the high-pressure fuel rail may crack and cause a fuel leak in the engine compartment, increasing the risk of fire. Dealers will replace the fuel rail free of charge.

    Product
    BMW — 2022 BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V511000·2023-08-07

    2021-2023 Tiffin Motorhomes Recalled for Propane Leak Risk

    Tiffin is recalling certain 2021-2023 Allegro and related motorhomes due to a defective LPG tank connection that may cause propane leaks and fire risk. Free inspection and repair are available through Tiffin dealers.

    Product
    TIFFIN — 2023 TIFFIN ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V516000·2023-08-07

    Audi Q8 and Q7 Fuel Pump Failure Risk Recall

    Volkswagen is recalling certain 2019-2021 Audi Q8 and 2020-2021 Audi Q7 vehicles due to a fuel pump component that may break, causing the pump to fail. A failed fuel pump can stall the engine, increasing crash risk.

    Product
    AUDI — 2021 AUDI Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V413000·2023-08-06

    Jeep Grand Cherokee Models Recalled for Detaching Rear Coil Springs

    Chrysler is recalling certain 2022-2023 Jeep Grand Cherokee and 2021-2023 Jeep Grand Cherokee L vehicles. Rear coil springs may detach while driving, creating a crash risk; dealers will repair them free.

    Product
    JEEP — 2021 JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V415000·2023-08-06

    2023 Hyundai Palisade brake booster defect may cause power brake loss

    Certain 2023 Hyundai Palisade vehicles have a brake booster defect that can cause loss of power brake assist, requiring longer stopping distances and increasing crash risk.

    Product
    HYUNDAI — 2023 HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V438000·2023-08-06

    School Bus Engine Control Module Defect May Cause Unexpected Shutdown

    Daimler Trucks recalls certain Thomas Built school buses (2020-2023) due to an engine control module defect that can cause unexpected engine shutdown while driving, increasing crash risk.

    Product
    THOMAS BUILT BUSES — 2021 THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V361000·2023-08-05

    2021-2022 Coachmen motorhomes recalled for cooktop gas leak risk

    Forest River is recalling 2021-2022 Coachmen motorhomes with defective cooktop burner valves that can develop gas leaks. The leaks pose a fire risk and will be remedied by free cooktop replacement.

    Product
    COACHMEN — 2022 COACHMEN BEYOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V365000·2023-08-05

    Mercedes-Benz Vehicles: Emergency Calling System Disabled by Software Error

    Mercedes-Benz USA is recalling certain 2017-2022 models after a communication module software error disabled the emergency eCall system. Owners can receive a free software update via over-the-air delivery or at a dealer.

    Product
    MERCEDES-BENZ — 2020 MERCEDES-BENZ AMG E63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V267000·2023-08-04

    Certain BMW Vehicles: Sunroof May Close Without Key Fob Present

    BMW is recalling 2019-2023 X5, X6, X7, and 4 Series vehicles because the sunroof may close without the key fob inside, creating injury risk. Dealers will reprogram the control unit free of charge.

    Product
    BMW — 2021 BMW X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V154000·2023-08-03

    2023-2024 International trucks recalled for loose battery box bolts

    Navistar is recalling certain 2023 and 2024 International trucks because battery box mounting bolts may be loose or missing. Loose bolts could allow the battery box to detach, creating a road hazard and increasing crash risk.

    Product
    INTERNATIONAL — 2023 INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V155000·2023-08-03

    Ford Recalls 2022-2023 Bronco for Steering Gear Lock-Up Defect

    Ford recalls 2022-2023 Broncos for steering gear damage that can lock up the steering wheel and cause loss of steering control, increasing crash risk.

    Product
    FORD — 2022 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide