Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 9,611
Critical: 161
Severe: 589
Most recent: 2026-09-24

Of the 9,611 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 589 (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.

7126–7150 of 9611

ModerateFDA (Devices)·Z-2274-2014·2014-08-27
AMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 TECNIS CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 12.0 and 12.5 Product Usage: AMO TECNIS CL monofocal foldab
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1548-2014·2014-08-27
US Compounding Recalls Mislabeled Ephedrine Sulfate Injection Syringes
US Compounding Inc is recalling 762 syringes of ephedrine sulfate injection due to a labeling error on the outer protective bags that could cause confusion regarding the drug's strength.
Product
ePHEDrine Sulfate Injection, USP 25 mg/5 mL (5 mg/mL) Single Use 5 mL Syringe, For IV, IM, or SC injection, Preservative Free, For Office/Hospital Use Only, Protect from Light, 62295-3084-05, US Compounding Pharmacy, Conway, AR 800-718-3588
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2277-2014·2014-08-27
AMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Power Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 TECNIS CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 15.5, 16.0 Product Usage: AMO TECNIS CL monofocal foldable
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2284-2014·2014-08-27
AMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling specific Tecnis CL intraocular lenses because they may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 23, 23.5 & 24. Product Usage: AMO TECNIS CL monofocal folda
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2281-2014·2014-08-27
AMO Tecnis CL Intraocular Lenses Recalled for Incorrect Diopter Power Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 Tecnis CL intraocular lenses because they may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 19.5-20 Product Usage: AMO TECNIS CL monofocal foldable IOL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2283-2014·2014-08-27
AMO TECNIS CL Foldable Silicone IOLs Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 TECNIS CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 21.5-22.5 Product Usage: AMO TECNIS CL monofocal foldable I
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2278-2014·2014-08-27
AMO Tecnis CL Intraocular Lenses Recalled for Incorrect Diopter Power Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 Tecnis CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 16.5, 17.0 Product Usage: AMO TECNIS CL monofocal foldable
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2264-2014·2014-08-27
Hyperion Medical Recalls HyperBlue 1530 Laser Brochures for Misleading Claims
Hyperion Medical is recalling brochures and website information for the HyperBlue 1530 laser because they promoted features not cleared by the FDA.
Product
All brochures printed before November 20, 2013 for the HyperBlue 1530 medical laser, including the product brochure and the online information regarding the product at www.hyperionMed.com before December 3, 2013.
Category
Medical Device
Distribution
10 states
LowFDA (Drugs)·D-1544-2014·2014-08-27
Triveen PRx RNF Capsules Recalled for Incorrect Vitamin B12 Labeling
Trigen Laboratories is recalling Triveen PRx RNF Capsules because the label lists Vitamin B12, which is not in the formulation.
Product
Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laboratories, Inc., Sayreville, NJ 08872, NDC 13811-558-30, UPC 3 13811 55830 2.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·14V515000·2014-08-26
Jayco Recalls 2015 Seismic Fifth Wheels for Incorrect Cargo Labels
Jayco is recalling 2015 Seismic fifth wheel trailers because incorrect cargo capacity labels may lead to overloading, tire failure, and crashes.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-2314-2014·2014-08-20
Interbake Recalls Mrs. Fields Cookies Due to Undeclared Walnuts
Interbake Foods LLC is recalling specific lots of Mrs. Fields Milk Chocolate Chip Cookies because some cartons contain undeclared walnuts.
Product
Mrs. Fields Milk Chocolate Chip Cookies, Net Wt. 8 oz (227 g) cardboard carton with 8 individually wrapped 1 oz cookies. 12 cartons in a case. UPC 8-86002-50651-7.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2183-2014·2014-08-20
Ortho-Clinical Diagnostics Recalls VITROS CA 19-9 Reagent Packs and Calibrators
Ortho-Clinical Diagnostics is recalling VITROS CA 19-9 Reagent Packs and Calibrators, Lot 1320, because they may produce positively biased results on specific VITROS systems.
Product
VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs, Lot 1320 VITROS¿ CA 19-9 Reagent Packs are used on VITROS¿ ECi/ECiQ Immunodiagnostic Systems, VITROS¿ 3600 Immunodiagnostic Systems and VITROS¿ 5600 Integrated Systems for the quantitative measurement of
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2312-2014·2014-08-20
Uncle Ben's Ready Rice Recalled for Undeclared Barley Gluten
Mars Food US is recalling Uncle Ben's Ready Rice Garden Vegetable pouches because some contain undeclared barley, a gluten source.
Product
Uncle Ben's(R) Ready Rice GARDEN VEGETABLE, with PEAS, CARROTS, AND CORN, NET WT. 8.8 OZ (250g), UPC 5480023334
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2190-2014·2014-08-20
Codman Certas Valve Recalled for Pressure Specification Clarification
Codman & Shurtleff is recalling 9,498 Codman Certas In Line Valves to clarify the pressure specification for the virtual off setting in the product's Instructions for Use.
Product
Codman Certas - In Line Valve with SIPHONGUARD¿, Unitized Catheter and Accessories; Product Code: 82-8806 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management
Category
Medical Device
Distribution
43 states
ModerateFDA (Food)·F-2315-2014·2014-08-20
Nutrition Express Recalls Lindberg B-Complex Vitamins for Folic Acid Labeling Error
Nutrition Express is recalling Lindberg B-Complex and Fitness Multi 1 vitamins because the folic acid content was found to be higher than the label claim.
Product
Lindberg B-Complex, 50mg, 60 capsules (UPC 092865236601), 120 capsules (UPC 092865236120), 240 capsules (UPC 092865236243).
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2185-2014·2014-08-20
Codman Certas Valve Recalled to Clarify Pressure Specifications in Instructions
Codman & Shurtleff is recalling 9,498 Codman Certas In Line Valves to clarify the pressure specification for the virtual off setting in the product's Instructions for Use.
Product
Codman Certas - In Line Valve with Catheter and Accessories; Product Code: 82-8801 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydrocephalus.
Category
Medical Device
Distribution
43 states
ModerateFDA (Food)·F-2317-2014·2014-08-20
Nutrition Express Recalls Vitamins Due to Excess Folic Acid Content
Nutrition Express is recalling specific vitamin products because the folic acid content was found to be higher than the amount stated on the label.
Product
Fitness Labs Fitness Multi 2, 90 capsules (UPC 654186946203) and 180 capsules (UPC 654186946227).
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-2318-2014·2014-08-20
Nutrition Express Recalls Lindberg B-Complex Vitamins for High Folic Acid
Nutrition Express is recalling Lindberg B-Complex vitamins because the folic acid content was found to be higher than the label claim.
Product
Lindberg B-Complex, 100mg, 60 capsules (UPC 092865239602), 240 capsules (UPC 092865239244),
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2171-2014·2014-08-20
Intuitive Surgical Recalls EndoWrist Stapler Manuals for pH Specification Change
Intuitive Surgical is recalling EndoWrist Stapler 45 User Manual Addenda and Wall Charts to correct the pH range specification for enzymatic cleaners.
Product
EndoWrist Stapler System User Manual Addendum and Wall Chart; The EndoWrist Stapler 45 System and EndoWrist Stapler 45 Reloads are intended to be used with the da Vinci Si Surgical System (Model IS3000) for resection, transection and/or creation of anastomoses in General, Gyn
Category
Medical Device
Distribution
2 states
ModerateFDA (Food)·F-2311-2014·2014-08-20
Frederick Farms Chocolate Ice Cream Cups Recalled for Wrong Lid
Garber Ice Cream Company is recalling Frederick Farms 4oz chocolate ice cream cups because the wrong lids were used during production.
Product
Frederick Farms 4oz chocolate ice cream cups, net wt. 67grams, 24 per box, 231 boxes per pallet, expiration 6-10-15
Category
Food
Distribution
4 states
ModerateFDA (Devices)·Z-2191-2014·2014-08-20
Codman Certas Valve Recalled for Pressure Specification Clarification
Codman & Shurtleff is recalling 9,498 Codman Certas valves to clarify the pressure specification for the virtual off setting in the product's Instructions for Use.
Product
Codman Certas - In Line Valve with SIPHONGUARD¿ Device, Unitized BACTISEAL¿ Catheter and Accessories; Product Code: 82-8807 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid)
Category
Medical Device
Distribution
43 states
ModerateFDA (Food)·F-2316-2014·2014-08-20
Nutrition Express Recalls Vitamins Due to Excess Folic Acid Content
Nutrition Express is recalling specific vitamin products because the folic acid content was found to be higher than the label claim.
Product
Fitness Labs Fitness Multi 1, 90 capsules (UPC 654186946555) and 180 capsules (UPC 654186946609).
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2186-2014·2014-08-20
Codman Certas Valve Recall Clarifies Pressure Specification in Instructions
Codman & Shurtleff is recalling 9,498 implantable valves to clarify the pressure specification for the virtual off setting in the Instructions for Use.
Product
Codman Certas - In Line Valve with Unitized Catheter and Accessories; Product Code: 82-8802 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydroceph
Category
Medical Device
Distribution
43 states
LowFDA (Devices)·Z-2176-2014·2014-08-20
Agfa Digital Radiography X-Ray System Recalled for Mislabeled Output Power
AGFA Healthcare Corp. is recalling one Agfa Digital Radiography X-Ray System DX-D 100 unit in West Virginia because it was mislabeled with a factory label showing 32 KW output power.
Product
Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with diagnoses.
Category
Medical Device
Distribution
1 state
LowFDA (Devices)·Z-2120-2014·2014-08-20
Nidek GYC-1000 Green Laser Photocoagulator Recalled for Missing Aperture Label
Nidek Inc is recalling 567 GYC-1000 Green Laser Photocoagulator systems because the required laser aperture label was not applied to the devices.
Product
GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser Photocoagulator Model GYC -1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation, iridotomy and trabeculoplasty.
Category
Medical Device
Distribution
Distributed nationwide