UnclassifiedAnnounced September 4, 2026
Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement
Products contain undeclared yohimbine
Read FDA’s announcement (opens in a new tab)Recalls affecting Mississippi
Data last updated: September 6, 2026 at 11:49 PM UTC
16,572 recalls foundJust announced
Straight from FDA press releases — not yet formally classified or risk-gradedUnclassifiedBacteria/virusAnnounced September 4, 2026
Foods Alive — Moringa Leaf Powder
Potential to be contaminated with Salmonella
Read 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
Read FDA’s announcement (opens in a new tab)UnclassifiedBacteria/virusAnnounced September 3, 2026
Great Value — Organic Triple Berry Blend
Possible E. Coli Contamination
Read 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
Read FDA’s announcement (opens in a new tab)UnclassifiedAnnounced August 31, 2026
Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement
Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)
Read 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
Read FDA’s announcement (opens in a new tab)UnclassifiedAllergenAnnounced August 31, 2026
Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.
Undeclared milk
Read 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.
Read FDA’s announcement (opens in a new tab)UnclassifiedBacteria/virusAnnounced August 29, 2026
Martina — Mangoes
Potential contamination with Salmonella
Read FDA’s announcement (opens in a new tab)Class IHigh risk
DrugRecalled June 18, 2020
Acadia Farms, Serenity, soothing mint, 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.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-1469-2020
- Lot/product code:
- FG003177
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
Class IHigh risk
DrugRecalled June 18, 2020
Goodness Gurus, Healthy Hemp Drops, 500MG/Berry, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 6 53341 99271 0
Chemical contamination: product contains elevated levels of not listed on the label lead.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-1460-2020
- Lot/product code:
- FG003236
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
Class IHigh risk
DrugRecalled 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.
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▸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
Class IHigh risk
DrugRecalled June 18, 2020
Tasty Drops Hemp Oil Extract, Vanilla, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76471 4
Chemical contamination: product contains elevated levels of not listed on the label lead.
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▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-1450-2020
- Lot/product code:
- FG003126
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
Class IHigh risk
DrugRecalled June 18, 2020
Tasty Drops, Hemp Oil Extract, Vanilla, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29086 6
Chemical contamination: product contains elevated levels of not listed on the label lead.
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▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-1477-2020
- Lot/product code:
- FG003144, FG003249
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
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
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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.
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
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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.
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.
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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
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)
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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.
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)
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▸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.
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
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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.
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.
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
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
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
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
Class IHigh risk
FoodRecalled April 3, 2021
ISOMORPH 28 PURE WHEY iSOLATE NEOPOLITAN ICE CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 8 11836 02251 3 & 5lb, UPC 8 11836 02252 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-0503-2021
- Lot/product code:
- 2lb - All EXP DATES up to and including 05/2021 5lb - All EXP DATES up to and including 05/2021
- Recalling firm:
- Hi Tech Pharmaceuticals
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
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
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".
▸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
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
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
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
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
Class IHigh risk
FoodRecalled 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.
▸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