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Recalls affecting Arizona

Data last updated: September 6, 2026 at 11:49 PM UTC

16,792 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
Wording
Class IHigh risk
DrugRecalled June 18, 2020

Recovery Releaf, Pure CBD Oil, Vanilla, 1000MG, 25MG per serving, 1 fl. oz (30 ml) bottles,Distributed by: Recovery Releaf, West Palm Beach, FL

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-1467-2020
Lot/product code:
FG003133
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Tasty Drops, Hemp Oil Extract, Natural, 1500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29088 0

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-1472-2020
Lot/product code:
FG003142, FG003247
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Herbzeedy, Hemp Oil Full Spectrum, Natural, 500 MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Herbzeedy, Statesboro, GA

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-1462-2020
Lot/product code:
FG003122, FG003123
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Made by Hemp 1000MG Hemp Extract, Strawberry Creme, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76554 4

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-1453-2020
Lot/product code:
FG003109
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 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
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
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
DrugRecalled 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
DrugRecalled 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
DrugRecalled 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
DrugRecalled 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
FoodRecalled 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.

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
FoodRecalled 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.

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
FoodRecalled 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.

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
FoodRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE COOKIES N CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89836 8 & 5lb, UPC 6 49241 87832 5 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.

Full report

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

Recall #:
F-0502-2021
Lot/product code:
2lb - All EXP DATES up to and including 10/2023 5lb - 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
FoodRecalled 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.

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
FoodRecalled 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.

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
FoodRecalled 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.

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)
Class IHigh risk
FoodRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE FUDGE POP DIETARY SUPPLEMENT NET WT. 2lb jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071 UPC 8 11836 02223 0

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

Full report

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

Recall #:
F-0499-2021
Lot/product code:
2lb - All EXP DATES up to and including 05/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89001 0 & 5lb, UPC 6 49241 87831 5 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.

Full report

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

Recall #:
F-0501-2021
Lot/product code:
2lb - All EXP DATES up to and including 06/2022 5lb - 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
FoodRecalled 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.

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)