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.

Which agencies issued them

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.

2976–3000 of 9607

ModerateFDA (Drugs)·D-0496-2019·2019-02-27
Advanced Pharma Recalls Fentanyl Syringes Due to Incorrect Expiration Date
Advanced Pharma Inc. is recalling 100 syringes of Fentanyl in 0.9% Sodium Chloride due to an incorrect expiration date on the label.
Product
Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0498-2019·2019-02-27
Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotency
Advanced Pharma Inc. is recalling 672 bags of Oxytocin 20 Units Injectable Solution because the product may contain higher concentrations than labeled.
Product
Oxytocin 20 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1002 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-703-99.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0499-2019·2019-02-27
Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotency
Advanced Pharma Inc. is recalling Oxytocin 30 Units Injectable Solution because the product may contain higher concentrations than labeled.
Product
Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0514-2019·2019-02-27
Mometasone Furoate Cream Recalled for NDC Typographical Error
ACP Nimble Buyer, Inc. is recalling Mometasone Furoate Cream due to a typographical error in the National Drug Code (NDC) on the label.
Product
Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0497-2019·2019-02-27
Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotent Drug Concerns
Advanced Pharma Inc. is recalling 12 bags of Oxytocin 10 Units Injectable Solution because the product may contain higher concentrations than labeled.
Product
Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0860-2019·2019-02-20
Salmon River Foods Recalls Forest Wild Dark Chocolate Bars for Undeclared Milk
Salmon River Foods is recalling Forest Wild Dark Chocolate bars due to undeclared milk. The product was distributed in Massachusetts and Wisconsin.
Product
The Forest Wild Collection Dark Chocolate bar, CB15052, net wt. 1.25 oz per bar. Product is packaged in a card board box of 12 individually wrapped chocolate bars. Dream Chocolate brand, UPC on each bar is 6 76181 15088 1. Label has the wolf image. The label is read in parts:
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-0485-2019·2019-02-20
Dr. Reddy's Recalls Levetiracetam Injection Due to Labeling Error
Dr. Reddy's Laboratories is recalling Levetiracetam Injection bags because the primary label incorrectly identifies the product strength and sodium chloride concentration.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM INJECTION)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0493-2019·2019-02-20
Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration
Tris Pharma is recalling specific lots of Infants' Ibuprofen because the medication may contain a higher concentration of ibuprofen than labeled.
Product
Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39338 3, NDC 59779-925-23.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0888-2019·2019-02-20
RXBAR Mixed Berry Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company is voluntarily recalling RXBAR Mixed Berry bars due to undeclared peanut. Consumers should stop eating the product and return it to the store.
Product
RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0859-2019·2019-02-20
Mylan Recalls DrNatura Probiotics and Detox Kits for Undeclared Soy
Mylan Pharmaceuticals is recalling DrNatura Flora Protect Probiotics and Toxinout Kits due to an undeclared soy allergen statement.
Product
DrNatura Toxinout Kit Broad Spectrum Detoxification Program
Category
Food
Distribution
0 states
HighFDA (Food)·F-0879-2019·2019-02-20
RXBAR Recalls Chocolate Sea Salt Bars Due to Undeclared Peanut
Chicago Bar Company LLC is voluntarily recalling Chocolate Sea Salt RXBARs because they contain undeclared peanut, a major food allergen.
Product
Chocolate Sea Salt RXBARs , 1.83 oz., single bar, , 12-count carton, 10-count carton, , 5-count carton, 4-count carton
Category
Food
Distribution
43 states
ModerateFDA (Drugs)·D-0998-2019·2019-02-20
Avella recalls magnesium sulfate bags with incorrect barcode expiration dates
Avella of Deer Valley is recalling 250 bags of compounded magnesium sulfate due to incorrect expiration dates in the 2D barcodes.
Product
MAGnesium 1gm sulfate, added to D5W 50 mL, Volume 52 mL, sterile single use bag, Compounded by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-901-05.
Category
Drug
Distribution
13 states
ModerateFDA (Drugs)·D-0482-2019·2019-02-20
US Compounding Recalls LET Gel 4% Syringes Due to Missing Lot and Expiration Dates
US Compounding Inc is recalling 1,931 syringes of LET Gel 4% because the labels are missing specific lot and expiration dates.
Product
LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0999-2019·2019-02-20
Avella Recalls Magnesium Sulfate Bags Due to Incorrect Barcode Expiration Dates
Avella of Deer Valley is recalling 4,950 bags of compounded magnesium sulfate because the 2D barcodes contain incorrect expiration dates that do not match the label.
Product
MAGnesium 2gm sulfate, added to D5W 50 mL, Volume: 54 mL, Sterile single use bag, Compounded by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-902-05.
Category
Drug
Distribution
13 states
ModerateFDA (Drugs)·D-1000-2019·2019-02-20
Avella recalls magnesium sulfate bags with incorrect barcode expiration dates
Avella of Deer Valley is recalling 8,500 bags of compounded magnesium sulfate because the 2D barcodes contain incorrect expiration dates that do not match the label.
Product
MAGnesium 2 gm sulfate, added to NS 50 mL, Sterile single use bag, 54 mL, Compounded by Avella Specialty Pharmacy 24416 N 19 th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-907-05.
Category
Drug
Distribution
13 states
ModerateFDA (Drugs)·D-0997-2019·2019-02-20
Avella Recalls Labetalol Syringes Due to Incorrect Barcode Expiration Dates
Avella of Deer Valley, Inc. is recalling 2,840 syringes of Labetalol 20mg Injectable Solution because the 2D barcodes contain incorrect expiration dates.
Product
Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-822-71.
Category
Drug
Distribution
13 states
LowFDA (Devices)·Z-0822-2019·2019-02-20
Luminex Recalls Verigene BC-GP Utility Kits Due to Labeling Error
Luminex Corporation is recalling Verigene BC-GP Utility Kits because they were incorrectly labeled with Amplification Tray labels.
Product
Vergene Amplification Tray - 700uL, BC-GP REF 20-011-018 The Verigene(R) Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the sample-to-result Verigene System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and identif
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0801-2019·2019-02-13
Funky Chunky LLC Recalls Nutty Choco Pop for Undeclared Allergens
Funky Chunky LLC is recalling Nutty Choco Pop because the label fails to declare that the product contains cashews and almonds.
Product
Nutty Choco Pop, 10 oz. bag. Sold in the following configurations: Item #101, Gift Box (contains 1-10 oz. bag), Item #1728 Holiday Crowd Pleaser (contains 5-10 oz. bags), and #9676 Crowd Pleaser (contains 5-10 oz. bags).
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0841-2019·2019-02-13
Bornstein Seafoods Recalls Unpasteurized Dungeness Crab Meat Due to TTI Error
Bornstein Seafoods is recalling unpasteurized Dungeness crab meat because incorrect Time Temperature Indicators were applied, potentially masking temperature abuse and allowing Clostridium botulinum growth.
Product
5-pound cans of unpasteurized, ready-to-eat, Dungeness crab meat, packaged in reduced oxygen metal cans that were shipped with Fresh-Check B Time Temperature Indicator (TTIs). Product was shipped frozen. The label is read in parts: "***BORNSTEIN SEAFOODS ***WILD Dungeness C
Category
Food
Distribution
2 states
HighFDA (Food)·F-0811-2019·2019-02-13
Mrs Grissom's Salads Recalls Pimento Cheese and Chicken Salad for Undeclared Milk
Mrs Grissom's Salads, Inc. is recalling 407 cases of Pimento Cheese and Cranberry Pecan Chicken Salad due to an undeclared milk allergen.
Product
Mrs GRISSOM'S SELECT OLD FASHIONED PIMENTO CHEESE**Mrs. GRISSOM'S SELECT CRANBERRY PECAN CHICKEN SALAD**INGREDIENTS: Sugar, Cider Vinegar, Water, Egg Yolks*** CONTAINS: Egg, Soy, Pecans
Category
Food
Distribution
3 states
LowFDA (Devices)·Z-0794-2019·2019-02-13
Ascension Radial Head Implant Recalled for Incorrect Instructions for Use
Ascension Orthopedics is recalling specific Radial Head Implants because they were packaged with instructions for a different product.
Product
Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number, MRH-350-04-WW
Category
Medical Device
Distribution
1 state
HighNHTSA·19V085000·2019-02-08
Forest River Cherokee Recalled for Incorrect Federal Tire Placard Information
Forest River is recalling 2019 Cherokee recreational trailers because the Federal Placards list incorrect tire size information, which may lead to the installation of insufficient tires.
Product
FOREST RIVER — FOREST RIVER CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V064000·2019-02-08
Isuzu and Chevrolet Trucks Recalled for Odometer Unit Display Error
Isuzu is recalling 2019 NPR and Chevrolet 4500/5500 trucks because the odometer may display kilometers instead of miles, potentially delaying critical maintenance.
Product
CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 4500, NRR, LOW CAB FORWARD 5500, NPR HD
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0765-2019·2019-02-06
Edwards Lifesciences Recalls Swan Ganz Catheters Due to Lumen Reversal
Edwards Lifesciences is recalling 459 Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings, potentially leading to misdiagnosis.
Product
Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 151F7 Product Usage: The Swan-Ganz Thermodilution Catheter provides a diagnostic tool for physicians to rapidly determine hemodynamic pressures and cardiac output when used with a compatible cardiac output computer.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-0763-2019·2019-02-06
Edwards Lifesciences Recalls Swan Ganz Catheters Due to Lumen Reversal
Edwards Lifesciences is recalling 875 units of Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings.
Product
Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 131F7P (5 pack of 131F7) Product Usage: The Swan-Ganz Thermodilution Catheter provides a diagnostic tool for physicians to rapidly determine hemodynamic pressures and cardiac output when used with a compatible cardiac o
Category
Medical Device
Distribution
0 states