State

New York product recalls

73,737 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,955
Critical: 1,508
Severe: 3,701
Most recent: 2026-10-28

Of the 12,955 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,701 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32351–32375 of 86692

ModerateFDA (Food)·F-1441-2020·2020-09-09
Sundial Princess Almaz Spiced Tea Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Sundial Princess Almaz Spiced Tea because it is misbranded and deemed an unapproved drug due to labeling claims.
Product
SUNDIAL PRINCESS ALMAZ Traditional ETHIOPIAN Organic SPICED TEA; "***Improves circulation***eliminates gas stomach griping & cramps. Relieves acid reflux, coughs, flu, hay fever, allergies, breaks up mucus and fights infection***" packaged in a breathable-type bag within a box.
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1469-2020·2020-09-09
Sundial Herbal Products Recalls Jamaican Milk Wiss Due to Misbranding
Sundial Herbal Products is recalling Jamaican Milk Wiss herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***JAMAICAN MILK WISS***2oz.***USES: REMOVES MUCOUS FROM THE BODY, TUMORS***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1454-2020·2020-09-09
Sundial Bitter Wood Herbal Product Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Bitter Wood herbal products under a court order because the labels make unapproved drug claims.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BITTER WOOD***2 oz.***USES: EXPELS WORMS IN THE WEST INTESTINES, DESTROYS PARASITES, LEUKEMIA, DESTROY APPETITE FOR ALCOHOL***"
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1483-2020·2020-09-09
Sundial Herbal Products Recalls Jack in the Bush Due to Misbranding
Sundial Herbal Products is recalling Jack in the Bush herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***JACK IN THE BUSH***1oz.***USES: COLD MEDICINE (ESP. IN CHILDREN), CALMS THE NERVES, RELIEVES DEPRESSION***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-2932-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 2,197 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1486-2020·2020-09-09
Sundial Broom Weed Herbal Product Recalled for Misbranding and Unapproved Drug Claims
Sundial Herbal Products is recalling Broom Weed herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BROOM WEED***1oz.***USES: BREAKS UP INFECTION IN BLADDER & REPRODUCTIVE SYTSEM, VENEREAL DISEASE, FEVER***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1473-2020·2020-09-09
Sundial Pimento Herbal Product Recalled for Misbranding and Unapproved Drug Claims
Sundial Herbal Products is recalling Pimento herbal products under a permanent injunction. The items are misbranded and deemed unapproved drugs due to specific labeling claims.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***PIMENTO***1 oz.***USES: STIMULANT, DIABETES, WORMS, PREVENTS STROKES, REDUCES TOBACCO URGE, WARMS BODY***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1455-2020·2020-09-09
Sundial Devil Horsewhip Herbal Product Recalled for Misbranding
Sundial Herbal Products is recalling Devil Horsewhip herbal products under a court order because the items are misbranded and considered unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***DEVIL HORSEWHIP***1 oz.***USES: COUGH, COLD, CHEST PAIN,***FEVER, VENEREAL DISEASE***"
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1456-2020·2020-09-09
Sundial Mango Leaf Herbal Product Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Mango Leaf herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***MANGO LEAF***1 oz.***USES: KIDNEY STONES, HIGH BLOOD PRESSURE, RELATED TO NERVOUS CONDITIONS***"
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2936-2020·2020-09-09
Diasorin Recalls Parvovirus B19 IgG EIA Kit Due to Labeling Error
Diasorin Inc. is recalling 615 units of the Parvovirus B19 IgG EIA kit because the printed label inside the box lid contains an incorrect Lot Specific Constant value.
Product
Parvovirus B19 IgG EIA kit Part No. V519IGUS
Category
Medical Device
Distribution
11 states
ModerateFDA (Food)·F-1452-2020·2020-09-09
Sundial Bay Leaves Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling bay leaves labeled with unapproved drug claims. The FDA determined the products are misbranded and unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BAY LEAVES***1 oz.***USES: COUGH, COLD, DIABETES, ACHES, PAINS, DIGESTION, FEVER, FLU SYMPTOMS***"; packaged in clear plastic zip-top bags
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2872-2020·2020-09-09
GE Healthcare Recalls OEC 9800 and 9900 C-Arms for Dose Display Issues
GE Healthcare is recalling 221 OEC 9800 and 9900 C-Arms because field service engineers changed the dose display to DAP, violating FDA regulations requiring AKR/CAK.
Product
The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during diagnostic, surgical and interventional procedures. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2933-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 13 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US and 2. FR4A-RCV-A0 EU - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1470-2020·2020-09-09
Sundial Spanish Needle Herbal Product Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Spanish Needle herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***SPANISH NEEDLE***1oz.***USES: HEART AILMENTS, DIABETES, LOWERS FEVER***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1489-2020·2020-09-09
Sundial Herbal Products Recalls Koromantee Colonic Cleaner as Unapproved Drug
Sundial Herbal Products is recalling Koromantee Colonic & Intestinal Cleaner because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Product
"SUNDIAL***KOROMANTEE***Colonic & Intestinal Cleaner***used by the descendants of the Koromantee people in Jamaica to help cleanse and strengthen the bowels, stomach, intestines, and colonic areas of the body.***" packaged in 16oz glass bottles
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1474-2020·2020-09-09
Sundial Herbal Products Recalls Piss A Bed for Unapproved Drug Claims
Sundial Herbal Products is recalling Piss A Bed herbal products under a permanent injunction because the products are misbranded and deemed unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***PISS A BED***1 oz.***USES: LIVER TONIC, ARTHRITIS, RHEUMATISM, KIDNEY, BLADDER, JAUNDICE***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1465-2020·2020-09-09
Sundial African Fever Bush Recalled for Misbranding and Unapproved Drug Claims
Sundial Herbal Products is recalling African Fever Bush under a permanent injunction because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***African Fever Bush***1oz***USES: FEVER, WORMS IN CHILDREN
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1499-2020·2020-09-09
Sundial Herbal Products Recalls Axum Ethiopian Honey Beverage
Sundial Herbal Products is recalling Axum Ethiopian Honey Beverage because it is misbranded and deemed an unapproved drug based on labeling claims.
Product
"AXUM ETHOIPIAN HONEY BEVERAGE***SUNDIAL HERBS***"
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1479-2020·2020-09-09
Sundial White Jointa Herbal Product Recalled for Misbranding
Sundial Herbal Products is recalling White Jointa herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***WHITE JOINTA***1 oz.***USES: NERVES, COLD, ASTHMA, BRONCHITIS, MUCOUS FEVER MENSTRUAL PROBLEMS***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1442-2020·2020-09-09
Sundial Moringa Leaf Powder Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Sundial Nigerian Moringa Leaf Powder because the product is misbranded and deemed an unapproved drug due to specific labeling claims.
Product
SUNDIAL NIGERIAN MORINGA LEAF POWDER; "***Anti-inflammatory, builds Red Blood cells***" 4oz and 8oz jars
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1443-2020·2020-09-09
Sundial Organic Jamaican Turmeric Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Sundial Organic Jamaican Turmeric because the product is misbranded and deemed an unapproved drug due to labeling claims.
Product
SUNDIAL ORGANIC JAMAICAN TUMERIC; "***increases the quality and quantity of breast milk***suppresses the development of parasite that causes tumors cancer, growths, cysts & all types of cancers***"
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1506-2020·2020-09-09
Sundial Herbal Products Recalls Talibah's Tooth Powder for Misbranding
Sundial Herbal Products is recalling Talibah's Tooth Powder because the product is misbranded and deemed an unapproved drug based on its labeling claims.
Product
"SUNDIAL***Talibah's Tooth Powder***"
Category
Drug
Distribution
1 state
ModerateFDA (Food)·F-1476-2020·2020-09-09
Sundial Purple Sage Herbal Product Recalled for Unapproved Drug Claims
Sundial Herbal Products is recalling Purple Sage herbal products under a permanent injunction because the labeling makes unapproved drug claims.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***PURPLE SAGE***1 oz.***USES: DEPRESSION, INSECT BITES, INSOMNIA, RELIEVES CONGESTION***"; packaged in clear plastic zip-top bags
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2930-2020·2020-09-09
Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component
Stimwave Technologies is recalling 1,424 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not referenced in product labeling.
Product
StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US and 2. FR4A-TR-BO - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1466-2020·2020-09-09
Sundial Herbal Products Recalls Mojo Bush Under FDA Injunction
Sundial Herbal Products is recalling Mojo Bush herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.
Product
"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***MOJO BUSH***1 oz.***USES: SKIN, BLOOD PURIFIER, STOMACH & INTESTINAL CLEANSER, REMOVES PARASITES***"; packaged in clear plastic zip-top bags
Category
Drug
Distribution
1 state