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.

2251–2275 of 9607

  • ModerateFDA (Devices)·Z-1249-2020·2020-02-26

    Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 1,360 units of the Arrow Epidural Catheterization Kit CK-02220 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL CATHETERIZATION KIT CK-02220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1262-2020·2020-02-26

    Abbott i-STAT CHEM8+ Cartridges Recalled for Lack of FDA Clearance

    Abbott Point Of Care Inc. is recalling i-STAT CHEM8+ cartridges because they are not FDA cleared and do not have CLIA waived status.

    Product
    i-STAT CHEM8+ cartridges (blue), List No. 09P31-25. UDI (01) 00054749001910 - Product Usage: The i-STAT CHEM8+ cartridge may be used for the quantitative measurement of sodium, potassium, chloride, blood urea nitrogen (BUN), ionized calcium, TCO2, glucose, creatinine, and hematoc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1243-2020·2020-02-26

    Arrow Central Venous Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 140 units of Central Venous Catheterization Kits because the product lidstock contains the incorrect expiration date.

    Product
    Arrow Central Venous Catheterization Kit ASK-04200-UPM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1247-2020·2020-02-26

    Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 1,760 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL CATHETERIZATION KIT JH-05500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1263-2020·2020-02-26

    Abbott i-STAT CG4+ Cartridges Recalled for Lack of FDA Clearance

    Abbott Point Of Care Inc. is recalling i-STAT CG4+ cartridges because they are not FDA cleared and lack CLIA waived status.

    Product
    i-STAT CG4+ cartridge (blue), List No. 03P85-50. UDI (01) 00054749002269 - Product Usage: The i-STAT CG4+ cartridge is intended for the quantitative measurement of lactate, pH, pCO2, and pO2 in venous, arterial or capillary whole blood.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1261-2020·2020-02-26

    Siemens Recalls Atellica CH High Sensitivity C-Reactive Protein Calibrator

    Siemens Healthcare Diagnostics is recalling Atellica CH High Sensitivity C-Reactive Protein Calibrators for in vitro diagnostic use.

    Product
    Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product Usage: For in vitro diagnostic use in the calibration of ADVIA¿ Chemistry systems for the CardioPhase¿ hsCRP assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1248-2020·2020-02-26

    Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 1,320 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL CATHETERIZATION KIT AM-05500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1245-2020·2020-02-26

    Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 870 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.

    Product
    Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1246-2020·2020-02-26

    Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 160 units of the Arrow Epidural Catheterization Kit (YC-02220) because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL CATHETERIZATION KIT YC-02220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1250-2020·2020-02-26

    Arrow Spinal Anesthesia Set Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 90 units of Arrow SPINAL ANESTHESIA SET ASA-25090-S because the product lidstock contains the incorrect expiration date.

    Product
    Arrow SPINAL ANESTHESIA SET ASA-25090-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1242-2020·2020-02-26

    Arrow PSI Kit Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc. is recalling 410 units of Arrow PSI Kits due to incorrect expiration dates on the product lidstock.

    Product
    Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1251-2020·2020-02-26

    Arrow Epidural Catheterization Component Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 540 units of the Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2020·2020-02-26

    Arrow International Recalls Tuohy Needles With Incorrect Expiration Dates

    Arrow International Inc is recalling 2,126 units of STIM and INSL CPNB Tuohy needles because the product lidstock contains the incorrect expiration date.

    Product
    (1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") AB-18140-N (2) Arrow¿ STIM CPNB TUOHY NDL: 18G x 11CM (4-3/8") AB-18110-N (3) Arrow¿ STIM CPNB TUOHY NDL: 18G x 8CM (3-1/8") AB-18080-N (4) Arrow¿ STIM CPNB TUOHY NDL: 17G x 8CM (3-1/8") AB-17080-N (5) Arrow¿ STIM CPNB T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1241-2020·2020-02-26

    Arrow StimuCath Continuous Nerve Block Kit Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 155 units of the StimuCath Continuous Nerve Block Kit because the product lidstock contains an incorrect expiration date.

    Product
    Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1239-2020·2020-02-26

    Arrow FlexTip Plus Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 1,150 units of FlexTip Plus Combined Spinal Epidural Catheterization Kits because the product lidstock contains the incorrect expiration date.

    Product
    Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1255-2020·2020-02-26

    Arrow PICC Kit Recalled for Incorrect Expiration Date on Lidstock

    Arrow International is recalling specific lots of PICC kits because the lidstock displays the wrong expiration date.

    Product
    Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1244-2020·2020-02-26

    Arrow Epidural Needle Component Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 1,839 units of Arrow Epidural Needle Component AN-05505 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL NEEDLE COMPONENT AN-05505
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0851-2020·2020-02-26

    Teva Recalls Tramadol Tablets Due to Incorrect Package Insert Labeling

    Teva Pharmaceuticals is recalling Tramadol Hydrochloride 50 mg tablets because the patient leaflets contain incorrect dosing instructions for unscored tablets.

    Product
    Tramadol Hydrochloride Tablets USP CIV, 50 mg, packaged in a) 100-count bottles (NDC 0093-0058-01), b) 500-count bottles (NDC 0093-0058-05), RX only, Manufactured in Czech Republic for: Teva Pharmaceuticals USA, Inc., North Wales, PA 19545
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1252-2020·2020-02-26

    Arrow Epidural Needle Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 180 units of the Arrow EPIDURAL NEEDLE KIT SL-05500 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL NEEDLE KIT SL-05500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0840-2020·2020-02-19

    Kushim Tablets Recalled for Unapproved Active Ingredients

    B and A Trading Corporation is recalling 40 packages of Kushim Tablets marketed without FDA approval. Analysis found the product contains unapproved active ingredients.

    Product
    Kushim Tablets (Gushim) 45-count packages, Label in foreign language
    Category
    Drug
    Distribution
    2 states