Hazard

Labeling recalls

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

What the numbers show

Total: 82
Critical: 0
Severe: 0
Most recent: 2026-02-18

Of the 82 labeling recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 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.

51–75 of 82

HighFDA (Food)·H-0364-2026·2025-12-24
Linzer heart cookies recalled over undeclared milk and a colour additive
Dough-To-Go is recalling 3,486 cases of Linzer Hearts Baked Cut Out Cookies over undeclared milk and FD&C Blue #1.
Product
Linzer Hearts Baked Cut Out Cookies UPC 0 44964 22072 2 72 - 4.0 oz Cut Cookies CBB-220-LZ Net Weight: 18 lbs Ingredients: Enriched flour (bleached WHEAT flowr, malted barley flour, niacin, iron, thaimine mononitrate, riboflavin, folic acid), butter (pasteurized cream (MILK), sal
Category
Food
Distribution
1 state
HighFDA (Food)·H-0303-2026·2025-12-17
Decaf coffee pods recalled because the boxes contained caffeinated pods
Gimme Coffee is recalling 252 boxes of gimme! Decaf de Agua coffee pods because the outer packaging is labelled decaf while the pods inside are caffeinated Deep Disco pods.
Product
Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods Inner-packaging/pod packaging: gimme! coffee Deep Disco caffeinated coffee pods
Category
Food
Distribution
10 states
ModerateFDA (Food)·H-0238-2026·2025-12-17
Matjes herring recalled over undeclared FD&C Red Number 40
Kosher First is recalling 283 units of Shloimy's Heimishe Matjes Herring over undeclared FD&C Red #40.
Product
Shloimy's Heimishe Matjes Herring packaged in 7oz plastic container
Category
Food
Distribution
1 state
HighFDA (Food)·H-0247-2026·2025-12-10
Dried red bayberry recalled over undeclared sulfites and cyclamates
Rong Shing Trading NY is recalling 10 cases of Aojia Dried Red Bayberry because the product contains undeclared sulfites at 7.39mg per serving, and cyclamates.
Product
Aojia Dried Red Bayberry; packaged in 5.6oz (160g) clear plastic bottle; UPC 6942514920327
Category
Food
Distribution
4 states
HighFDA (Food)·H-0223-2026·2025-12-10
Asian wing sauce recalled over undeclared soy in 4,888 bottles
Blonde Beard's is recalling 4,888 8 oz bottles of Dojo Asian Wing Sauce because the product contains undeclared soy.
Product
Blonde Beard's Dojo Asian Wing Sauce, wing sauce hot sauce condiment, shelf stable, 2 years, glass bottle, 8 oz, Blonde Beard s. Responsible firm on label: Blonde Beard s 2230 S Braun Ct Lakewood, CO 80228.
Category
Food
Distribution
31 states
HighFDA (Food)·H-0226-2026·2025-12-10
Blackened shrimp recalled over undeclared sulfite in three lots
Pacific Seafood is recalling 15,498 lbs of Raw Blackened Shrimp because the shrimp may contain 3.4mg sulfur dioxide per serving and the label does not declare sulfite.
Product
Pacific Seafood Raw Blackened Shrimp Peeled & Deveined Tail-Off, refrigerated, farm-raised. Net wt. per tray 8 oz (227 g). UPC 0 27241 44630 5. Ingredients: Shrimp (Shrimp, Water, Salt, Sodium tripolyphosphate (to retain moisture), Blackened Seasoning (Sea Salt, Paprika, Spice
Category
Food
Distribution
3 states
HighFDA (Food)·H-0227-2026·2025-12-10
Chocolate ice cream bars recalled over undeclared wheat in one lot
Dreyer's Grand Ice Cream is recalling 3,410 cases of Haagen-Dazs mini chocolate dark chocolate ice cream bars over undeclared wheat.
Product
Retail Box: Haagen-Dazs mini chocolate dark chocolate ice cream bars 6 BARS/11.1 FL/OZ(328mL) INGREDIENTS: CHOCOLATE ICE CREAM: CREAM, SKIM MILK, SUGAR, COCOA PROCESSED WITH ALKALI, EGG YOLKS. DARK CHOCOLATE AND VEGETABLE OIL COATING: DARK CHOCOLATE (SUGAR, CHOCOLATE, SOY LECITHI
Category
Food
Distribution
4 states
HighFDA (Food)·H-0230-2026·2025-12-10
Frozen lava buns recalled because milk is not declared on the label
Prime Food Processing is recalling 2,243 cases of frozen Lava Bun with Salted Egg Yolk because the products do not declare milk in the Contains statement or the ingredient statement.
Product
Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted butter and cream are listed in the ingredient statement.
Category
Food
Distribution
33 states
HighFDA (Food)·H-0229-2026·2025-12-10
Green tea lava buns recalled because milk is not declared
Prime Food Processing is recalling frozen Lava Bun with Green Tea Flavor because the products do not declare milk in the Contains statement or the ingredient statement.
Product
Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the ingredient statement.
Category
Food
Distribution
33 states
ModerateFDA (Devices)·Z-2324-2025·2025-08-20
Anorectal manometry kit outer label shows the manufacturing date as expiry
Zvu Anorectal Manometry Procedure Kits are being recalled because the outer kit label carries an incorrect expiration date, with the manufacturing date used in its place. 8 kits are affected.
Product
Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2298-2025·2025-08-20
Ultra IABP catheter kits carry indications not reviewed by the FDA
Insightra Ultra IABP Catheter Kits are being recalled because the device carries indications and compatibility claims not reviewed by the FDA, and its instructions are inconsistent with product training.
Product
Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Catheter Kit Model/Catalog Number: IMU7F-40, IMU7F-35, IMU7F-30, IMU7F-25, and IMU7F-20 Software Version: Not applicable Product Description: The Insightra Ultra IABP Catheter Kit is a 7 French catheter available wi
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2265-2025·2025-08-13
T4 Total ELISA kit box expiry exceeds the standards' shelf life
T4 Total ELISA kits are being recalled because the expiration date on the kit box label and Certificate of Analysis exceeded the shelf life of the standards and control solutions by two months. 47 units affected.
Product
Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Model/Catalog Number: EIA-4568 Product Description: T4 Total ELISA
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2231-2025·2025-08-06
3M Ranger irrigation fluid warming set notice clarifies flow rates
The 3M Ranger Irrigation Fluid Warming Set is subject to a notice issued to clarify flow rates related to the inlet fluid temperature. 186,880 units are affected.
Product
3M Ranger Irrigation Fluid Warming Set, REF 24750
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2146-2025·2025-07-30
Ellik Evacuator non-locking cone has conflicting sterilization instructions in Japan
The Cone with Male Tubing, Non-Locking, Ellik Evacuator, model 191-NRS, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Cone with Male Tubing, Non-Locking, Ellik Evacuator. Model Number: 191-NRS. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2139-2025·2025-07-30
Reusable endoscope silicone seals have conflicting sterilization instructions in Japan
Blue Silicone Reusable Silicone Seals 6-12 FR, model CS-B612, are being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silicone seals fit over the biopsy port of endoscopes to seal off the working channel. Some contain a lumen which allows instruments to be passed through the seal and minimize or prevent fl
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2145-2025·2025-07-30
Ellik Evacuator locking adapter has conflicting sterilization instructions in Japan
The Ellik Evacuator Adapter, Locking, model 190-NRS, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 5 units affected.
Product
Ellik Evacuator Adapter, Locking. Model Number: 190-NRS. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2141-2025·2025-07-30
Ellik Evacuator glass body has conflicting sterilization instructions in Japan
The Glass Body for the 194 Ellik Evacuator, model 190A, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2142-2025·2025-07-30
Ellik Evacuator male connector tubing has conflicting sterilization instructions in Japan
The Tubing for Male Connector 194, Ellik Evacuator, model 190-4, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2144-2025·2025-07-30
Ellik Evacuator latex bulb has conflicting sterilization instructions in Japan
The Ellik Latex Bulb, model 194-2, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 48 units affected.
Product
Ellik Latex Bulb, Ellik Evacuator. Model Number: 194-2. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2140-2025·2025-07-30
Green endoscope silicone seals have conflicting sterilization instructions in Japan
Green Silicone Seals for Accessories, reusable 0-7 FR, model CS-G7, are being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU.
Product
Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The reusable silicone seals fit over the biopsy port of endoscopes to seal off the working channel. Some contain a lumen which allows instruments to be passed through the seal and mini
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2143-2025·2025-07-30
Ellik Evacuator recalled over conflicting sterilization instructions in Japanese inserts
The Ellik Evacuator, model 194, is being recalled because of discrepancies between the Japanese language package insert sterilization instructions and the manufacturer's IFU. 11 units are affected.
Product
Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2094-2025·2025-07-16
TrueDent White dental resin cartridges carry an expiration date formatting error
TrueDent White dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 109 units are affected.
Product
TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2093-2025·2025-07-16
TrueDent Yellow dental resin cartridges carry an expiration date formatting error
TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.
Product
TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2090-2025·2025-07-16
TrueDent Clear dental resin cartridges carry an expiration date formatting error
TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.
Product
TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2092-2025·2025-07-16
TrueDent dental resin cartridges carry a formatting error in expiration dates
TrueDent Magenta dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 94 units are affected.
Product
TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances
Category
Medical Device
Distribution
Distributed nationwide