Hazard

Class Ii recalls

1,428 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 1,428
Critical: 0
Severe: 0
Most recent: 2026-07-08

Of the 1,428 class ii 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 class ii 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.

301–325 of 1428

HighFDA (Food)·H-1017-2026·2026-06-10
Albertsons apple waldorf salad does not declare walnut allergen
Albertsons store-made Apple Waldorf Salad is being recalled because the contains statement does not declare walnut. 33 units are affected.
Product
UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WALDORF FS UPC 27169500000 Kitchen SALAD APPLE WALDORF LRG UPC 27170300000 Kitchen SALAD APPLE WALDORF MED UPC 27169300000 Kitchen SALAD APPLE…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2026·2026-06-10
Stapes prosthesis pistons carry an incorrect functional length on labeling
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.
Product
TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0982-2026·2026-06-10
Pavilions single serve banana nut muffins do not declare walnut
Pavilions Banana Nut Muffins single serve, an Albertsons store-made item, are being recalled because the contains statement does not declare walnut. 55 units are affected.
Product
UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2292-2026·2026-06-10
Arvis Hip and Knee 3.0 trackers may show wear and corrosion
Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.
Product
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0994-2026·2026-06-10
Albertsons Twisted Bliss pretzel trays do not declare almond allergen
Albertsons store-made Twisted Bliss Pretzel Tray is being recalled because the contains statement does not declare almond. Two units are affected.
Product
UPC 29344500000 TWISTED BLISS PRETZEL TRAY This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0996-2026·2026-06-10
Imitation crab and shrimp sriracha salad does not declare pollock
Albertsons store-made Imitation Crab and Shrimp Salad Sriracha is being recalled because the contains statement does not declare pollock. 15 units are affected.
Product
UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2026·2026-06-10
Phothera 200 phototherapy calibration certificates had outputs reversed
Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.
Product
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1015-2026·2026-06-10
Imitation Cajun crab seafood salad does not declare crab and pollock
Albertsons store-made Seafood Salad Imitation Cajun Crab is being recalled because the contains statement does not declare crab and pollock. 53 units are affected.
Product
UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2205-2026·2026-06-10
ARTIS pheno systems may display zero dose while dose is applied
ARTIS pheno interventional fluoroscopic X-ray systems are being recalled because they may sporadically display a zero X-ray dose even though an actual dose is applied to the patient.
Product
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system
Category
Medical Device
Distribution
0 states
HighFDA (Drugs)·D-0576-2026·2026-06-10
Equaline extra strength antacid tablets contain small metallic particles
Equaline Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID — EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1044-2026·2026-06-10
Albertsons ready meals meatloaf does not declare anchovy allergen
Albertsons store-made Ready Meals Meatloaf is being recalled because the contains statement does not declare anchovy. 353 units are affected.
Product
UPC 21409600000 READY MEALS MEATLOAF SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1035-2026·2026-06-10
Albertsons large spring salad does not declare almond allergen
Albertsons store-made Kitchen Salad Spring Large is being recalled because the contains statement does not declare almond. 25 units are affected.
Product
UPC 29787500000 KITCHEN SALAD SPRING LARGE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0575-2026·2026-06-10
GoodSense ultra strength antacid tablets contain small metallic particles
GoodSense Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT — GOODSENSE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1026-2026·2026-06-10
Albertsons Cheeses of France platter does not declare almond
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.
Product
UPC 27837800000 PLATTER CHEESES OF FRANCE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0569-2026·2026-06-10
Family Wellness ultra strength antacid tablets contain metallic particles
A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.
Product
FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2279-2026·2026-06-10
CASE cardiac testing systems may spark at the printer head
CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.
Product
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1021-2026·2026-06-10
Albertsons grilled chicken salad does not declare almond allergen
Albertsons store-made Kitchen Salad Grilled Chicken is being recalled because the contains statement does not declare almond. 27 units are affected.
Product
UPC 27163100000 Kitchen SALAD GRILLED CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0988-2026·2026-06-10
Albertsons 16-inch carving tray does not declare walnut
An Albertsons store-made 16-inch carving tray is being recalled because the contains statement does not declare walnut. 12 units are affected.
Product
UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1032-2026·2026-06-10
Albertsons pork meat pies do not declare anchovy allergen
Albertsons store-made pork meat pies are being recalled because the contains statement does not declare anchovy. 790 units in total are affected.
Product
UPC 21176300000 MEAT PIE PORK 4CT SS COLD UPC 21025900000 PIE PORK FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2281-2026·2026-06-10
Covidien EndoStitch loading unit pouches may have sterility-breaking holes
Covidien EndoStitch Polysorb Single Use Loading Units are being recalled because holes in the pouch may compromise the sterile barrier. 2,448 units are affected.
Product
Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0577-2026·2026-06-10
Equaline ultra strength antacid tablets contain small metallic particles
Equaline Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF — EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0968-2026·2026-06-10
Albertsons gourmet Dubai cookies do not declare pistachio
Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.
Product
UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0579-2026·2026-06-10
TopCare ultra strength antacid tablets contain small metallic particles
TopCare Health Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT — TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0578-2026·2026-06-10
TopCare extra strength antacid tablets contain small metallic particles
TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE EXTRA STRENGTH ANTACID — TOPCARE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2026·2026-06-10
BD Pyxis Anesthesia Station fingerprint scanner may overheat and burn
The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.
Product
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide