Hazard

Class I Recall recalls

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

What the numbers show

Total: 35
Critical: 0
Severe: 35
Most recent: 2026-04-08

Of the 35 class i recall recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 35 (100%) 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 i recall 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.

26–35 of 35

SevereFDA (Devices)·Z-1545-2026·2026-03-18
TRUE METRIX manuals recalled as Class I over E-5 error code guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX Kit/RE4001-01, Leader TRUE METRIX Kit/RE4002-01, Leader TRUE METRIX Meter Only/RE4002-40, CVS TRUE METRIX Kit/RE4007-01SB, GN
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0388-2026·2026-03-11
Silintan herbal pills recalled as Class I for undeclared meloxicam
123Herbals is recalling Silintan 25-count pill bottles because FDA analysis revealed the presence of undeclared meloxicam. The FDA has classified this recall as Class I.
Product
SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1470-2026·2026-03-11
Abiomed Impella RP Flex recalled as Class I over sensor drift
Abiomed is recalling the Impella RP Flex with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Product
Impella RP Flex with SmartAssist. Product Code: 1000323.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1469-2026·2026-03-11
Abiomed Impella RP with SmartAssist recalled as Class I
Abiomed is recalling the Impella RP with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Product
Impella RP with SmartAssist. Product Code: 0046-0035.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0396-2026·2026-03-11
Mojo Max Fusion capsules recalled as Class I over undeclared drug ingredients
Mojo Max Fusion XXX capsules are being recalled because FDA analysis revealed undeclared sildenafil at 13.1 mg per capsule and tadalafil at 13.8 mg per capsule. The FDA has classified this recall as Class I.
Product
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0397-2026·2026-03-11
MR. 7 Super capsules recalled as Class I over undeclared sildenafil
StuffbyNainax is recalling MR. 7 SUPER 700000 capsules because FDA analysis revealed the presence of undeclared sildenafil and tadalafil. The FDA has classified this recall as Class I.
Product
MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
Category
Drug
Distribution
0 states
SevereFDA (Devices)·Z-1471-2026·2026-03-11
Abiomed Impella RP recalled as Class I over sensor malfunction risk
Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Product
Impella RP. Product Code: 0046-0011.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0531-2026·2026-03-04
Frozen fish balls recalled as Class I for undeclared wheat and sesame
Min Jiang Food Store, trading as Koi Koi Trading, is recalling frozen Fish Ball in 400 g packs because of undeclared wheat and sesame. The FDA has classified this recall as Class I.
Product
Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0530-2026·2026-03-04
Frozen fish balls 200g recalled as Class I for undeclared allergens
Min Jiang Food Store, trading as Koi Koi Trading, is recalling frozen Fish Ball in 200 g packs because of undeclared wheat and sesame. The FDA has classified this recall as Class I.
Product
Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0519-2026·2026-03-04
Dried croaker fish recalled as Class I because it is uneviscerated
Prime Food Processing is recalling Dried Croaker Fish, 8 oz, because the fish is uneviscerated. The FDA has classified this recall as Class I, its most serious category.
Product
Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER FISH); DISTRIBUTED BY: PFP LLC, Brooklyn, NY, 11211, USA; Product must be thoroughly cleaned and cooked before consumption.; PRODUCT OF VIETNAM; UPC: 6 946976 81
Category
Food
Distribution
18 states