The Recall Desk

Archive

September 2023 recalls

423 recalls were announced in September 2023.

What the numbers show

Critical
4
Severe
65
High
298
Moderate
54
Low
2

Of the 423 recalls this month scored against our rubric, 1% are Critical, 15% are Severe.

Which agencies issued them

401–423 of 423

  • HighFDA (Drugs)·D-1111-2023·2023-09-06

    Cardioplegia Solution Recalled Due to Lack of Sterility Assurance

    Central Admixture Pharmacy Services recalls Cardioplegia Solution due to inadequate validation of sterilization processes. One lot (36-262881) distributed nationwide may not be assured sterile.

    Product
    Cardioplegia Solution, low K, Maintenance 4:1 Plasmalyte, Low Potassium, total volume = 1047 mL, EVA Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0211-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1117-2023·2023-09-06

    Neonatal TPN Starter Bag Recalled Over Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling 104 neonatal TPN starter bags (Lot 36-260022) due to lack of validation data for sanitization cycles, which could compromise sterility assurance in this IV medication.

    Product
    Neonatal TPN Starter Bag, Amino Acids (trophamine) 3%/Dextrose 5% with CALCIUM and HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043. NDC: 72196-0419-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2477-2023·2023-09-06

    FDA Recalls Siemens epoc BGEM Crea Test Cards for Inaccurate Glucose Results

    Siemens Healthcare is recalling epoc BGEM Crea Test Cards that may produce inaccurate glucose readings in lower-range samples. 473 units were distributed to US facilities and international locations. No injuries reported.

    Product
    epoc BGEM Crea Test Card with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor Configuration 41.1
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-2473-2023·2023-09-06

    Diagnostic reagent kit recall: potential test result inaccuracy

    Siemens is recalling Atellica CH diagnostic reagent kits due to potential reagent carryover that could produce inaccurate test results. This may affect quality control and patient test reliability.

    Product
    Atellica CH Gamma-Glutamyl Transferase-IIn vitro diagnostic use in the quantitative determination of gamma-glutamyl transferase in human serum and plasma (lithium heparin Test Code: GGT Siemens Material Number (SMN): 11097597
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2023·2023-09-06

    Atellica CH Triglycerides Diagnostic Kit Recalled for Reagent Carryover

    Siemens Healthcare Diagnostics is recalling 11,824 units of Atellica CH Triglycerides test kits due to reagent carryover from other test parameters that can affect magnesium measurement accuracy. The FDA classified this as a Class II recall.

    Product
    Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the quantitative measurement of triglycerides in human serum and plasma (lithium heparin, potassium EDTA) using the Atellica CH Analyzer SMN: 11097591
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1142-2023·2023-09-06

    Sabril (vigabatrin) oral solution recalled for cross-contamination

    Lundbeck LLC recalls Sabril (vigabatrin) oral solution nationwide due to potential cross-contamination. The recall affects 10,543 cartons.

    Product
    SABRIL — SABRIL (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1269-2023·2023-09-06

    Siemens Atellica CH Total Protein II Recalled for Reagent Carryover

    Siemens Healthcare Diagnostics is recalling Atellica CH Total Protein II due to reagent carryover affecting magnesium test accuracy. The recall covers all lots (13,071 units) distributed nationwide and internationally.

    Product
    Atellica CH Total Protein II- In vitro diagnostic use in the quantitative determination of total protein in human serum and plasma (lithium heparin) using the Atellica CH Analyzer. SMN: 11097604
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1466-2023·2023-09-06

    Gourmet Garden Herbs Recalled for Improper Temperature Storage

    C & S Wholesale Grocers is recalling 29,469 cases of Gourmet Garden herb and spice products sold at Stop & Shop stores in the New York Metro region due to improper temperature storage. Consumers should discard these products.

    Product
    The following items sold at Stop & Shop stores located in the New York Metro Region: Gourmet Garden Jalapeno Groumet Garden Roasted Garlic Gourmet Garden Italian Herb Gourmet Garden Parsley Blend Gourmet Garden Cilantro Gourmet Garden Ginger Gourmet Garden Chunky Garlic Gourmet
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1486-2023·2023-09-06

    Grape Juice Recalled for Bloating in Sealed Cups

    Lyons Magnus LLC is recalling GFS Harvest Valley Grape Juice in 4 fl oz cups due to signs of bloating in containers. Consumers in multiple states should not consume and should dispose of the product safely.

    Product
    GFS Harvest Valley Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
    Category
    Food
    Distribution
    13 states
  • LowFDA (Drugs)·D-1139-2023·2023-09-06

    Clindamycin Phosphate Topical Solution Recalled for Defective Container

    Contract Pharmaceuticals is recalling Clindamycin Phosphate Topical Solution USP 1% due to defective containers that leak under the cap. The recall affects 11,350 bottles distributed nationwide.

    Product
    Clindamycin Phosphate Topical Solution USP, 1%, 60 mL bottle, Rx only, Manufactured by: Contract Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, Manufactured for: Glasshouse Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, NDC# 71428-003-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V618000·2023-09-05

    Wilson Recalls One 2024 DWH-750 Trailer for Tire Pressure Loss

    Wilson Trailer Company is recalling one 2024 DWH-750 Pacesetter Grain trailer because the tire pressure regulation system may fail at speeds over 45 mph, increasing crash risk.

    Product
    WILSON — WILSON DWH-750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V617000·2023-09-05

    Peterbilt and Kenworth trucks recalled for fuel hose production defects

    Remote Stage 2 fuel filter hoses in 2023-2024 Peterbilt and Kenworth trucks may be damaged, risking disconnection, engine stall, and fuel leaks that could cause fire or crashes.

    Product
    KENWORTH — KENWORTH, PETERBILT T280, T380, 536, 537
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·041-2023·2023-09-05

    AJC International Recalls Frozen Raw Pork Imported Without Reinspection

    AJC International is recalling approximately 17,428 pounds of frozen raw pork products that were imported into the United States without undergoing required reinspection.

    Product
    AJC International, Inc. Recalls Frozen, Raw Pork Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V616000·2023-09-05

    PACCAR Recalls 2023 Kenworth and Peterbilt Trucks for Driveshaft Defect

    PACCAR is recalling 2023 Kenworth K270, K370, and Peterbilt 220 trucks because the driveshafts can break under certain loading conditions, increasing the risk of a crash.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, K370, 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E066000·2023-09-05

    Covercraft Seat Covers Recalled for Incorrect Air Bag Deployment Risk

    Covercraft is recalling specific seat covers for Toyota, Ford, and Buick vehicles because incorrect thread may cause side-seat air bags to deploy incorrectly, increasing injury risk.

    Product
    SEATS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·039-2023·2023-09-02

    Hillshire Brands Recalls Smoked Sausage Due to Bone Fragments

    Hillshire Brands is recalling smoked sausage products due to possible bone fragment contamination. One oral injury has been reported.

    Product
    The Hillshire Brands Company — Hillshire Brands Company Recalls Smoked Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    7 states
  • SevereUSDA FSIS·040-2023·2023-09-02

    Banquet Frozen Chicken Strips Recalled for Plastic Contamination

    Conagra Brands is recalling Banquet Chicken Strips Meal due to possible plastic contamination that caused an oral injury.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — ConAgra Brands Inc. Recalls Banquet Brand Frozen Chicken Strips Entree Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V613000·2023-09-01

    Audi Recalls 2023 E-Tron GT Models for Battery Fire Risk

    Audi is recalling 2023 RS E-Tron GT and E-Tron GT vehicles because insufficient battery sealant may allow liquid accumulation, increasing the risk of electrical arcing and fire.

    Product
    AUDI — AUDI RS E-TRON GT, E TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V615000·2023-09-01

    2023 Porsche Taycan battery sealant defect increases fire risk

    Porsche is recalling 2023 Taycan vehicles with high-voltage batteries that may have insufficient sealant, allowing liquid accumulation that can cause electrical arcing and fire risk. Dealers will test and replace batteries free of charge.

    Product
    PORSCHE — PORSCHE TAYCAN TURBO S CROSS TURI, TAYCAN, TAYCAN CROSS TURISMO, TAYCAN TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V612000·2023-09-01

    2022 Silver Lake Travel Trailers Recalled for Detaching Sidewall Siding

    Forest River's 2022 Silver Lake and Della Terra travel trailers are being recalled because the aluminum sidewall siding may not be properly installed and could detach. Detached siding increases the risk of a crash or injury while towing.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide

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