Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 9,610
Critical: 161
Severe: 588
Most recent: 2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

6201–6225 of 9610

HighFDA (Food)·F-3049-2015·2015-09-02
Veggie Evolution Kale Crisps Recalled for Undeclared Milk Allergen
It Takes A Village Foods is recalling Veggie Evolution Kale Crisps Lemon Parmesan because the label lists Parmesan cheese but fails to declare milk as an allergen.
Product
Kale Crisps Lemon Parmesan sold under brand Veggie Evolution, each plastic package has a net weight 1.5 oz. There are six packages per case. UPC is 7 94504 69431 4. The product's label is read in part: "***VEGGIE EVOLUTION***KALE CRISPS***LEMON PARMESAN***INGREDIENTS: KALE,
Category
Food
Distribution
22 states
HighFDA (Devices)·Z-2455-2015·2015-09-02
Omnilife Recalls Offset Femoral Alignment Guides Due to Incorrect Markings
Omnilife Science Inc. is recalling 15 Offset Femoral Alignment Guides because the markings are reversed, which may prevent proper alignment during surgery.
Product
Offset Femoral Alignment Guide 4mm x 6¿; Product Code: KS 67024 Product Usage: The instrumentation has been designed to facilitate bone preparation and implantation of the Apex Knee or Apex Hip Systems. Product Usage: The instrumentation has been designed to facilitate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-3055-2015·2015-09-02
Vic's Original White Popcorn Recalled for Undeclared Milk Allergen
Barrel O' Fun Snack Foods is recalling one lot of Vic's Original White Popcorn because it contains an undeclared milk allergen.
Product
Vic's All Natural Original White Popcorn, Net Wt. 1-1/8 oz (32g), UPC 46555-00062
Category
Food
Distribution
6 states
HighFDA (Food)·F-3048-2015·2015-09-02
Veggie Evolution Kale Crisps Recalled for Undeclared Soy
It Takes A Village Foods is recalling Veggie Evolution Kale Crisps Zen Nori because the product contains soy, which is not declared on the label.
Product
Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly pouch has a net weight 1.5 oz. There are six packages per case. UPC is 7 13757 57480 8. The product's label is read in part: "***VEGGIE EVOLUTION***KALE CRISPS*
Category
Food
Distribution
22 states
HighFDA (Devices)·Z-2446-2015·2015-09-02
Roche cobas b 123 Fluid Pack Recall for Low PO2 Results
Roche is recalling 82 cobas b 123 Fluid Packs due to a calibration issue that may cause erroneously low PO2 results in patient samples.
Product
cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a fully automated POC system for whole blood in vitro measurement of pH, blood gases (B3G), electrolytes NAT, K+, iCaWt (ISE), hematocrit (THct), metabolites (GLu, Lac) total hemoglob
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2459-2015·2015-09-02
Advanced Sterilization Products Recalls CIDEX Activated Dialdehyde Solution
Advanced Sterilization Products is recalling CIDEX Activated Dialdehyde Solution because it may lack adequate data to support its 24-month shelf life.
Product
CIDEX Activated Dialdehyde Solution, 4 bottles/case, P/N: 2266
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1369-2015·2015-09-02
Mucinex Fast-Max DM Max Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast-Max DM Max bottles because the back label is missing active ingredients and safety warnings.
Product
MUCINEX FAST-MAX DM MAX AND MUCINEX NIGHTTIME COLD AND FLU — MUCINEX FAST-MAX DM MAX AND MUCINEX NIGHTTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND TRIPROLIDINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2472-2015·2015-09-02
Baxter MiniCap Peritoneal Dialysis Transfer Set Labeling Recall
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets to update labeling with safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Product Code: 5C4482. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and disconnections are perf
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2460-2015·2015-09-02
ASO Recalls Carepak Bandages Due to Unlabeled Benzalkonium Chloride
ASO, LLC is recalling Carepak Sheer Adhesive Bandages because 5/8 bandages contain 0.1% Benzalkonium Chloride, which is not listed on the label.
Product
Carepak Sheer Adhesive Bandages 50 Sterile Bandages Assorted Sizes
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-2442-2015·2015-09-02
Medtronic Guardian Real-Time Monitor Recalled for Finnish Translation Error
Medtronic MiniMed is recalling 254 Guardian Real-Time Monitors distributed in Finland due to a language translation error that reverses the on-screen labels for LOW and HIGH glucose alerts.
Product
Guardian Real-Time Monitor, Model No. CSS7100. Indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, in adults (18 years and older) with diabetes mellitus, for the purpose of improving diabetes management.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2441-2015·2015-09-02
Iris Diagnostics Recalls iChemVELOCITY Urine Chemistry Systems for Labeling Error
Iris Diagnostics is recalling iChemVELOCITY Automated Urine Chemistry systems because they do not maintain the claimed 5-day strip stability under specified conditions.
Product
iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049, 800-3050, 800-3079, 800-3080, 800-3530, 800-7167, 800-7190, 800-7713,800-7714, 800-7719, 800-7720. An in vitro diagnostic device used to automate the urine chemistry analysis profile using iChemVELOCITY Urine Chemistry
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2468-2015·2015-09-02
Stryker recalls mislabeled 5mm trocar sleeves due to length discrepancy
Stryker Sustainability Solutions is recalling 90 reprocessed trocar sleeves labeled as 100mm but containing 75mm models.
Product
Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery, Inc. Excel Trocar Sleeve w/Stability Sleeve 5mm x 100mm Reprocessed by Stryker Sustainability Solutions Product Usage: The Reprocessed Ethicon ENDOPATH¿ XCEL Universal Trocar Stability Sleeve is a sterile si
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2474-2015·2015-09-02
Baxter Recalls CAPD Solution Transfer Sets for Labeling Revisions
Baxter Healthcare Corp. is recalling 35,460 units of CAPD Solution Transfer Sets to update labeling with additional safety instructions and warnings.
Product
CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160. intended for use with containers of DIANEAL peritoneal dialysis solution.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2473-2015·2015-09-02
Baxter MiniCap Extended Life PD Transfer Set Labeling Recall
Baxter Healthcare Corp. is recalling 33,474 units of MiniCap Extended Life PD Transfer Sets to update labeling with additional safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and disconnections are performed at the transfer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-3054-2015·2015-09-02
Nepali Finger Chips Recalled for Undeclared Tartrazine
Balajee Trade Link LLC is recalling Rato Bhale Nepali Finger Chips because the product contains undeclared tartrazine (yellow #5).
Product
Rato Bhale Nepali Finger Chips Product of Nepal Weight: 200g (7.05 OZ) Imported by: Balajee Trade Link, LLC, PA USA Batch No. 01-15
Category
Food
Distribution
9 states
ModerateFDA (Devices)·Z-2453-2015·2015-09-02
BD CD56 PE Cy 7 Reagent Recalled for Unexpected Staining Patterns
Becton, Dickinson and Company is recalling three lots of CD56 PE Cy 7 reagent because they contain a low amount of HLA-DR PE antibody, which could result in an unexpected staining pattern.
Product
BD CD56 PE Cy 7: NCAM16.2 ASR Analyte Specific Reagent, Catalog number 335809 Hematology: The CD 56 antigen promotes homophilic adhesion in neurons and may be involved in homophilic adhesion of NK cells.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2471-2015·2015-09-02
Baxter Recalls MiniCap Peritoneal Dialysis Transfer Sets for Labeling Updates
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets to update labeling with new safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set Extra Short (4") with Twist Clamp. Product Code: 5C4483. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and disconnect
Category
Medical Device
Distribution
Distributed nationwide
LowUSDA FSIS·118-2015·2015-08-31
Holten Meat Recalls Beef Patties Due to Unlabeled MSG
Holten Meat Inc. is recalling approximately 501,509 pounds of Extra Value Meats Quarter Pound Beef Patties because monosodium glutamate (MSG) was used but not listed on the label.
Product
Branding Iron Holdings - Holten Meat — Recall Notification Report 118-2015 (Beef Patties)
Category
Food
Distribution
Distributed nationwide
ModerateUSDA FSIS·115-2015·2015-08-27
Swanson Recalls Boneless Beef Tender Tips Due to Undeclared Allergens
Swanson Meats is recalling approximately 20,063 pounds of boneless beef tender tips because the labels failed to declare soybean oil, MSG, and papain.
Product
Swanson Meat Co. — Recall Notification Report 115-2015 (Boneless Beef Tender Tips)
Category
Food
Distribution
Distributed nationwide
HighUSDA FSIS·114-2015·2015-08-26
California Qi Li's Recalls Duck Products Due to Undeclared Allergens
California Qi Li's Braised Chicken is recalling approximately 6,644 pounds of duck head and neck products because they contain undeclared soy and wheat allergens.
Product
California Qi Li's Braised Chicken Recalls Duck Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
1 state
HighFDA (Food)·F-2964-2015·2015-08-26
Freedom Snacks Sea Salt Caramel Popcorn Recalled for Undeclared Milk
Freedom Snacks is recalling 50 bags of Sea Salt Caramel Gourmet Popcorn because milk is not declared on the label, posing a risk to consumers with milk allergies.
Product
Sea Salt Caramel Gourmet Popcorn, sold under brand Freedom Snacks, packaged in a flexible plastic bag, net wt. 10 oz.. There is NO UPC. The product is labeled in parts: "***FREEDOM SNACKS***SEA SALT CARAMEL Gourmet Popcorn***Ingredients: popcorn, sugar, brown sugar, corn syru
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2402-2015·2015-08-26
Winco Inverness Recliners Recalled for Fire Retardant Foam Mislabeling
Winco Mfg. is recalling 29 Inverness recliners because the foam was mislabeled as fire retardant but is actually standard foam.
Product
Winco Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2396-2015·2015-08-26
Winco Drop Arm Care Cliner Chairs Recalled for Fire Retardant Mislabeling
Winco Mfg., LLC is recalling Drop Arm Care Cliner chairs because the foam was mislabeled as fire retardant but is actually standard foam.
Product
Winco Drop Arm Care Cliner Standard - with Steel Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2389-2015·2015-08-26
Stryker Triathlon X3 Tibial Bearing Insert Recall Due to Labeling Error
Stryker is recalling 10 units of Triathlon X3 Tibial Bearing Inserts because one unit was found in a pack labeled for a different model.
Product
Stryker Orthopaedics Triathlon X3 Tibial Bearing Insert - CR REF 5530-G-209 (component of the Triathlon Total Knee System) for fixation to the tibial baseplates via a locking wire mechanism.
Category
Medical Device
Distribution
4 states
LowFDA (Devices)·Z-2431-2015·2015-08-26
Cepheid Recalls Xpert CT/NG Vaginal and Endocervical Specimen Collection Kits
Cepheid is recalling Xpert CT/NG Vaginal/Endocervical Specimen Collection Kits because some lots contain a sub-component with an earlier expiration date than the kit itself.
Product
Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number CT/NGSWAB-50; Microbiology: The Cepheid X pert CT /NG Vagina Endocervical/ Specimen Collection Kit is designed to collect, preserve and transport patient Chlamydia trachomatis and Neisseria gonorrhoeae DN
Category
Medical Device
Distribution
Distributed nationwide