The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

3551–3575 of 9607

  • ModerateFDA (Devices)·Z-1910-2018·2018-05-30

    Baxter EXACTAMIX Inlets Recalled for Incorrect Over-Labeling

    Baxter Healthcare is recalling specific lots of EXACTAMIX Inlets due to incorrect over-labeling that may display blank or extended expiration dates.

    Product
    Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175 Usage: Exacta-Mix 2400 Compounding System Administration set is a disposable component of a compounding device used in the pharmacy to compound multiple source ingredients into one final solution.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1902-2018·2018-05-30

    Smith & Nephew Recalls Genesis II Knee Bushings Due to Labeling Error

    Smith & Nephew is recalling 18 units of Genesis II knee bushings because the left and right sides were incorrectly laser marked.

    Product
    smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING, REF CATALOG NUMBER 71440014 The GENESIS II Knee System Components are indicated for rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight, and activ
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1911-2018·2018-05-30

    Baxter EXACTAMIX Inlets Recalled for Incorrect Labeling

    Baxter Healthcare is recalling specific lots of EXACTAMIX Inlets due to incorrect over-labeling that may display blank or extended expiration dates.

    Product
    Baxter EXACTAMIX Inlet, Syringe Inlet, REF H938176 Usage: Exacta-Mix 2400 Compounding System Administration set is a disposable component of a compounding device used in the pharmacy to compound multiple source ingredients into one final solution.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1909-2018·2018-05-30

    Baxter EXACTAMIX Inlets Recalled for Incorrect Over-Labeling

    Baxter Healthcare is recalling specific lots of EXACTAMIX Inlets due to incorrect over-labeling that may display extended expiration dates.

    Product
    Baxter EXACTAMIX Inlet, Vented, High-Volume Inlet, REF H938174 Usage: Exacta-Mix 2400 Compounding System Administration set is a disposable component of a compounding device used in the pharmacy to compound multiple source ingredients into one final solution.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1912-2018·2018-05-30

    Spinal Elements Recalls Omega Lumbar Interbody Fusion Devices

    Spinal Elements is recalling 19 Omega Lumbar Interbody Fusion Devices because they were assembled with components that do not match the labeled lordosis angle.

    Product
    AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 The OmegaLIF(TM) (LIF(TM)) Expandable Lumbar Interbody Device is designed for use in intervertebral body spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) at o
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0826-2018·2018-05-30

    Exela Pharma Recalls Diclofenac and Misoprostol Tablets Due to Labeling Error

    Exela Pharma Sciences LLC is recalling 5,256 bottles of Diclofenac Sodium and Misoprostol tablets because some bottles were mislabeled with the wrong dosage.

    Product
    Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg, 60-count bottle, Rx Only, Manufactured by: Cipla Ltd., India; For: EAGLE PHARMACEUTICALS, INC., Woodcliff Lake, NJ 07677 USA, NDC 42367-111-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1919-2018·2018-05-30

    LivaNova Inspire 8 Integrated Phisio OXY Recall for Incorrect UDI Expiration Date

    LivaNova USA is recalling 70 units of Inspire 8 Integrated Phisio OXY devices because the expiration date in the UDI barcode is printed in the wrong format.

    Product
    Inspire 8 Integrated Phisio OXY w/ HVR Reservoir, Sterile EO, Catalog # 050714 The intended uses for the two elements that constitute the oxygenator/reservoir integrated devices are: INSPIRE 8M Hollow Fiber Oxygenator: The INSPIRE 8M is intended for use in adult and small adu
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1908-2018·2018-05-30

    Baxter EXACTAMIX Inlets Recalled for Incorrect Over-Labeling

    Baxter Healthcare is recalling specific lots of EXACTAMIX Inlets due to incorrect over-labeling that may display extended expiration dates.

    Product
    Baxter EXACTAMIX Inlet, Non-Vented, High-Volume Inlet, REF H938173 Product Usage: Exacta-Mix 2400 Compounding System Administration set is a disposable component of a compounding device used in the pharmacy to compound multiple source ingredients into one final solution.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1920-2018·2018-05-30

    Implant Direct Legacy 4 Implant Recalled for Mislabeling

    Implant Direct Sybron Manufacturing is recalling 18 units of Legacy 4 Implants due to a mislabeled vial cap. The main label was correct, but the cap showed the wrong part number.

    Product
    ImplantDirect Legacy 4 Implant, 5.7mmD x 5.7mmD Platform, Part 885708, Rx, Sterile. The incorrect cap label shows part 855708, 5.7mmD Platform, 8mmL.
    Category
    Medical Device
    Distribution
    10 states
  • LowFDA (Devices)·Z-1918-2018·2018-05-30

    LivaNova Inspire 6 Integrated Phisio OXY Recall for Incorrect UDI Expiration Date

    LivaNova USA is recalling 42 units of Inspire 6 Integrated Phisio OXY devices because the expiration date in the UDI barcode is printed in the wrong format.

    Product
    Inspire 6 Integrated Phisio OXY w/ HVR Reservoir, Sterile EO, Catalog # 050713 The intended uses for the two elements that constitute the oxygenator/reservoir integrated devices are: INSPIRE 6M Hollow Fiber Oxygenator: The INSPIRE 6M is intended for use in adult and small adul
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-1454-2018·2018-05-23

    eBars Recalls Organic Dark Cocoa Raspberry Bars for Peanut Allergen

    eBars is recalling 26,180 units of TRIM Organic Dark Cocoa Raspberry bars because they tested positive for peanut, an allergen not declared on the label.

    Product
    TRIM ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00423 1
    Category
    Food
    Distribution
    40 states
  • HighFDA (Food)·F-1451-2018·2018-05-23

    eBars Recalls Run Organic Chocolate Almond Bars for Peanut Allergen

    eBars is recalling Run Organic Chocolate Almond bars because they tested positive for peanut, an allergen not declared on the label.

    Product
    RUN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00404 2
    Category
    Food
    Distribution
    40 states
  • HighFDA (Food)·F-1441-2018·2018-05-23

    Market District Roasted Salted Cashews Recalled for Undeclared Allergens

    Kanan Enterprises is recalling Market District Roasted Salted Cashews because the product contains almonds and pecans that are not listed on the label.

    Product
    Market District Roasted Salted Cashews Whole Fancy Net WT 26 oz (1LB 10 OZ) 737g. Ingredients: Cashews, Canola and/or Peanut Oil, Salt. Distributed by Giant Eagle, Inc. Pittsburgh, PA 15238-2809 UPC 0 30034 10382 8
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1449-2018·2018-05-23

    eBars Recalls Organic Chocolate Peanut Bars for Undeclared Almond Allergen

    eBars is recalling HEAL Organic Chocolate Peanut bars because testing revealed the presence of undeclared almond allergen.

    Product
    HEAL ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00439 4
    Category
    Food
    Distribution
    40 states
  • HighFDA (Food)·F-1452-2018·2018-05-23

    eBars Recalls Organic Dark Cocoa Raspberry Bars for Undeclared Peanut Allergen

    eBars is recalling 2,903 units of RUN Organic Dark Cocoa Raspberry bars because testing revealed the presence of peanut, an allergen not declared on the product label.

    Product
    RUN ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00412 7
    Category
    Food
    Distribution
    40 states
  • HighFDA (Food)·F-1453-2018·2018-05-23

    eBars Recalls Trim Organic Chocolate Almond Bars for Peanut Allergen

    eBars is recalling Trim Organic Chocolate Almond bars because they tested positive for peanut, an allergen not declared on the label.

    Product
    TRIM ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00423 0
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1892-2018·2018-05-23

    Southmedic Recalls Sterile Scalpels Labeled as Non-Sterile

    Southmedic, Inc. is recalling 3,300 sterile disposable scalpels because the product contains non-sterile items labeled as sterile.

    Product
    Southmedic Sterile Disposable Scalpel Rx only Scalpels are intended to be used in various medical procedures for preparation, scraping and/or cutting of tissue.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-1442-2018·2018-05-23

    Zoi Mixed Berry Greek Yogurt Parfait Recalled for Coconut Labeling Error

    A G Specialty Foods is recalling Zoi Mixed Berry Greek Yogurt Parfaits because coconut is listed in ingredients but missing from the 'Contains' statement.

    Product
    Zoi Mixed Berry Greek Yogurt Parfait, 9 oz. clear plastic cup, covered with a clear plastic snap-on lid. UPC 8 17203 02172 1. The label is read in parts: "***Honey Greek Yogurt Willamette Valley Mixed Berries Honey Almond Granola Parfait***KEEP REFRIGERATED***INGREDIENTS: HONE
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1810-2018·2018-05-23

    Tosoh HbA1c Calibrator Recalled for Potential Inaccurate Patient Results

    Tosoh Bioscience Inc is recalling HbA1c Calibrators because they may cause erroneous patient test results.

    Product
    Tosoh ST AIA-PACK HbA1c Calibrator, HbA1c Calibrator, PN 025318 The product is intended for In Vitro Diagnostic Use Only for the calibration of the HbA1c Assay.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1868-2018·2018-05-23

    Richard Wolf Tube Set for TEM Recalled for Potential Tube Mixing

    Richard Wolf GmbH is recalling 1,710 units of the Tube Set for TEM (Ref 4170.801) because tube ends may be mixed up.

    Product
    RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1475-2018·2018-05-23

    Van's Gluten Free Waffles Recalled for Missing Allergen Labeling

    Van's gluten free Original 6 Waffles are being recalled because the ingredient statement failed to list milk and wheat.

    Product
    Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOY FLOUR),***RICE FLOUR,***SUNFLOWER AND/OR SOY LECITHIN***CONTAINS: SOY DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS SAN DIEGO, CA 92154 UPC 0
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-1890-2018·2018-05-23

    Convatec Esteem Synergy Stomahesive Skin Barrier Recalled for Size Defect

    ConvaTec is recalling 200 boxes of Esteem Synergy Stomahesive skin barriers because the stoma hole is larger than the 22mm size specified on the label.

    Product
    Convatec Esteem(TM) Synergy Stomahesive(R), 7/8 in. / 22mm, REF 405475 Product Usage: Esteem Synergy Stomahesive with Flexible Collar 22mm Precut Skin Barrier is used together with Esteem Synergy pouches as an ostomy system intended for the management of stomal output.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0806-2018·2018-05-23

    Prescript Pharmaceuticals Recalls Acetaminophen and Codeine Tablets for Labeling Error

    Prescript Pharmaceuticals is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because the storage temperature instructions on the label differ from the original manufacturer's declaration.

    Product
    ACETAMINOPHEN AND CODEINE PHOSPHATE — ACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN AND CODEINE PHOSPHATE)
    Category
    Drug
    Distribution
    1 state