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Recalls affecting Rhode Island

Data last updated: September 7, 2026 at 12:15 AM UTC

16,151 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

▸Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

▸Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

▸Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

▸Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

▸Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

▸Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
NewestOldest
High riskLow riskAll
Wording
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Road Suite 1, Saginaw, MI 48603

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1454-2020
Lot/product code:
FG003106
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

SP, hemp oil, Berry, 300MG CBD,1 FL. OZ (30 ML) bottles, Distributed by: The Spiffy Piff

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1465-2020
Lot/product code:
FG003277
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Made by Hemp 1000MG Hemp Extract, French Vanilla, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76553 7

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1451-2020
Lot/product code:
FG003107
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Acadia Farms, Equilibrium, vermont maple, 300 MG Hemp Oil, 1 Fl OZ (30 ML) bottles, Distributed by: Acadia Farms, Rehobeth, Massachusetts

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1468-2020
Lot/product code:
FG003181
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 27, 2020

Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC 52376-021-02; b) 4 fl oz (118 mL) NDC 52376-021-04, Sunstar Americas, Inc.

Microbial Contamination of Non-sterile Products: contamination with Burkholderia lata.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0103-2021
Lot/product code:
Lot #: a) C170FY, C170FZ, C170GA, C170GB, C170GC, C177GP, C177GQ, C177GR, Exp 6/30/2022; C191KS, C191KT, C191KU, C191KW, C191KX, C191KY, C198LJ, C198LK, C198LL, C198LM, C205BH, C205BJ, C205BK, C205BL, C205BM, C205BN, Exp 7/31/2022; C219DK, C219DL, C219DM, C219DN, C219DP, C219DQ, C219DR, C219DS, Exp 8/31/2022; C240GM, C240GP, C240GQ, C240GR, Exp 9/30/2022; b) C191KR, Exp 7/31/2020
Recalling firm:
Sunstar Americas, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 17, 2020

ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270 measured sprays, Distributed by Ndal Laboratories, 449 Alvarado St., Monterey, CA 93940 (bottle); NDAL MFG Inc., 80 Garden Court, Suite 100, Monterey, CA 93940 (carton); UPC 8 58631 00212 8. the Alvarado St. is for the bottle by putting "(bottle); NDAL MFG Inc., 80 Garden Court, Suite 100, Monterey, CA 93940 (carton); UPC 8 58631 00212 8." (according to the label)

Microbial Contamination of Non-Sterile Products: Product confirmed to have yeast

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0269-2021
Lot/product code:
LOT # 2010045; Best Before 10 2023
Recalling firm:
NDAL Mfg Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 27, 2021

Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 63629-1064-01), b) 60-count bottles (NDC 63629-1064-02), c) 90-count bottles (NDC 63629-1064-03), Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0303-2021
Lot/product code:
a) Lot #: 148969, Exp 7/31/2022, b) Lot #: 148791, Exp 7/31/2022, c) Lot #: 148991, Exp 7/31/2022
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 2, 2021

Enoxaparin Sodium Injection, USP 120 mg/ 0.8 mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 0.8 mL Single Dose Syringes Rx Only,Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-0796-4 UPC 360505079543 (carton) NDC 60505-0796-0 UPC (01)10360505079602 (label)

Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL (corresponding to 100 mg/mL strength) instead of 150 mg/mL (corresponding to 120 mg/0.8mL strength)

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0262-2021
Lot/product code:
Batch: CT003 Exp. 05/2022
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 2, 2021

Enoxaparin Sodium Injection, USP 100 mg/mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 1 mL Single Dose Syringes Rx Only, Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-0795-4 UPC 360505079544 (carton) NDC 60505-0795-1 UPC (01)10360505079510 (label)

Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength)

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0261-2021
Lot/product code:
Batch: CS008 Exp. 04/2022
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 17, 2021

Real Alkalized Water, concentrate. 4 oz. glass bottle . Drinkrealwater.com

FDA was notified of cases of acute liver failure after consumption of Real Water

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0482-2021
Lot/product code:
All codes
Recalling firm:
Real Water, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 17, 2021

Real Alkalized Water, packed in 16.9 oz., 1 Liter, 1.5 Liter, 1-Gallon and 5-Gallon plastic bottles. Drinkrealwater.com

FDA was notified of cases of acute liver failure after consumption of Real Water

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0481-2021
Lot/product code:
Real Water 16.9 oz., UPC (Case): 6-69149-10551-1, UPC (Single): 6-69149-10550-4 Real Water 1 Liter, UPC (Case): 6-69149-10553-5, UPC (Single): 6-69149-10552-8 Real Water 1.5 Ltr, UPC (Case): 6-69149-10555-9, UPC (Single): 6-69149-10554-2 Real Water 1 Gallon, UPC (Case): 6-69149-10561-0, UPC (Single): 6-69149-10560-3 ALL CODES of all products.
Recalling firm:
Real Water, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil and sildenafil, two FDA approved drugs making it an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0688-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil, an FDA approved drug making this an unapproved drug for which the safety and efficacy has not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0686-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil sildenafil, and vardenafil, FDA approved drugs making them an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0687-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil and sildenafil, two FDA approved drugs making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0685-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT. 5lb, UPC 6 49241 87837 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0507-2021
Lot/product code:
5lb - All EXP DATES up to and including 11/2022
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89856 6 & 5lb, UPC 6 49241 87833 9 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0504-2021
Lot/product code:
2lb - All EXP DATES up to and including 12/2022 5lb - All EXP DATES up to and including 12/2022
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

IFN iFORCE NUTRITION MASS GAINZ PROTEIN MATRIX BROWN SUGAR MAPLE OATMEAL COOKIE NET WT 2.2 KG/4.85 LBS container UPC 8 19500 01010 1 Mfg. For Dist. By Trib?????? Enterprises, LLC Vista, CA 92081

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label egg, milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0510-2021
Lot/product code:
4.85lb - All EXP DATES up to and including 01/2024 10lb - All EXP DATES up to and including 09/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT. 2LB, UPC 6 49241 89886 5 & 5lb, UPC 6 49241 87836 0 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0508-2021
Lot/product code:
2lb - All EXP DATES up to and including 09/2023 5lb - All EXP DATES up to and including 12/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 3, 2021

HI-TECH PHARMACEUTICALS PRECISION PROTEIN COOKIES & CREAM NET WT 2lbs (907g) container UPC 8 11836 02341 1 & 5lbs. (2.2kg) UPC 8 11836 02349 7 manufactured by Hi-Tech Pharmaceuticals, 6015-B Unity Dr. Norcross, GA

During an inspection by the FDA the firm was notified by FDA that the product contains contains wheat but the label states it is "Gluten Free".

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0511-2021
Lot/product code:
2lb - All EXP DATES up to and including 12/2022 5lb - All EXP DATES up to and including 10/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241 87829 2 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0498-2021
Lot/product code:
2lb - All EXP DATES up to and including 07/2021 5lb - All EXP DATES up to and including 03/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE MILKSHAKE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89876 4 & 5lb, UPC 6 49241 87830 8 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0500-2021
Lot/product code:
2lb - All EXP DATES up to and including 04/2023 5lb - All EXP DATES up to and including 04/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE SMORES DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89002 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0505-2021
Lot/product code:
2lb - All EXP DATES up to and including 06/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE HONEY GRANOLA DIETARY SUPPLEMENT NET WT. 2LB, UPC 8 11836 02303 9 & 5lb, UPC 8 11836 02302 2 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0509-2021
Lot/product code:
2lb - All EXP DATES up to and including 02/2023 5lb - All EXP DATES up to and including 10/2022
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE STRAWBERRY MILKSHAKE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89866 5 & 5lb, UPC 6 49241 87835 3 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0506-2021
Lot/product code:
2lb - All EXP DATES up to and including 11/2022 5lb - All EXP DATES up to and including 05/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)