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 New Mexico
Data last updated: September 6, 2026 at 11:49 PM UTC
16,220 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 September 10, 2012
HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-3888-21
Stronger than it should be (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in stronger than it should be assays of both the hydrocodone and acetaminophen components.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-057-2013
- Lot/product code:
- Lot number: C1440512A, Exp 12/13
- Recalling firm:
- Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
Class IHigh risk
DrugRecalled July 2, 2015
Zero Xtreme High Performance Fat Burner capsules, 30-count bottle, Distributed by Xtreme Z Distributors, Inc., Miami, FL 33180
Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed the presence of sibutramine and desmethylsibutramine.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-1165-2016
- Lot/product code:
- Lot 1220062085, Exp. 09/16
- Recalling firm:
- XTREME Z DISTRIBUTORS INC
Class IHigh risk
DrugRecalled July 13, 2015
Akttive High Performance Fat Burner Gold dietary supplement capsules, 30-count bottle, Distributed by Life and More, L.L.C., Doral, Florida
Marketed Without An Approved NDA/ANDA: Dietary supplements contains not listed on the label sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0664-2016
- Lot/product code:
- Lot # 000815004400; Exp 12/17
- Recalling firm:
- Life and More LLC
Class IHigh risk
DrugRecalled August 27, 2015
MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules per carton, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 0911312397354.
Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain not listed on the label thiosildenafil, an analogue of an FDA approved drug for male erectile dysfunchtion making this product an unapproved drug.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0229-2016
- Lot/product code:
- All lots through Expiration Date 06/01/2018
- Recalling firm:
- The One Minute Miracle Inc
Class IHigh risk
DrugRecalled August 27, 2015
MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7 538073516768.
Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain not listed on the label phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0230-2016
- Lot/product code:
- All lots through Expiration Date 04/15/2018
- Recalling firm:
- The One Minute Miracle Inc
Class IHigh risk
DrugRecalled December 23, 2015
APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0667-2016
- Lot/product code:
- All lots
- Recalling firm:
- Nuway Distributors, LLC
Class IHigh risk
DrugRecalled March 18, 2016
8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0865-2016
- Lot/product code:
- Lot # 56-148-EV, Exp 8/1/2017
- Recalling firm:
- Hospira Inc.
Class IHigh risk
DrugRecalled March 23, 2016
Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.
Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-1137-2016
- Lot/product code:
- Lot #: 50-343-DK*, Exp 01FEB2017; note that the lot number may be followed by numbers from 01 to 99.
- Recalling firm:
- Hospira Inc.
Class IHigh risk
DrugRecalled April 2, 2016
Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014
Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0918-2017
- Lot/product code:
- Lot # 22016, Exp 1/30/2017
- Recalling firm:
- Complete Pharmacy and Medical Solutions LLC
Class IHigh risk
DrugRecalled August 4, 2016
Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1159-02
Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0218-2017
- Lot/product code:
- Lot # 59064DK, Exp. 11/17
- Recalling firm:
- Hospira Inc., A Pfizer Company
Class IHigh risk
DrugRecalled March 12, 2017
EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0690-2017
- Lot/product code:
- US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017; lot 6GM088, exp. Oct 2017; lot 6GM087, exp. Oct 2017; lot 6GM198, exp. Oct 2017; lot 6GM081, exp. Sep 2017; lot 6GM091, exp. Oct 2017; lot 6GM199, exp. Oct 2017: INTERNATIONAL: lot 5FA665, exp. April 2017; lot 5GU763, exp. May 2017; lot 6FA293, exp. Oct 2017; lot 6FA292, exp. Oct 2017; lot 6GH294, exp. Oct 2017.
- Recalling firm:
- Meridian Medical Technologies a Pfizer Company
Class IHigh risk
DrugRecalled March 12, 2017
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0691-2017
- Lot/product code:
- US lot 5GN767, expiration April 2017; lot 5GN773, expiration April 2017; lot 6GN215, expiration Sep 2017: INTERNATIONAL lot 5GR765, expiration March 2017; lot 5GK771, expiration April 2017; lot 5ED824, expiration April 2017; and lot 6ED117, expiration ***
- Recalling firm:
- Meridian Medical Technologies a Pfizer Company
Class IHigh risk
DrugRecalled April 21, 2017
Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10
Presence of Particulate Matter: human hair found within an internal sample syringe.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0862-2017
- Lot/product code:
- Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02
- Recalling firm:
- Hospira Inc.
Class IHigh risk
FoodRecalled March 6, 2018
Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce; Net Wt. 18 oz. bottle; UPC Code 0 7561654383 8
Not listed on the label soy and wheat ingredients
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- F-0978-2018
- Lot/product code:
- All lots
- Recalling firm:
- Piggie Park Enterprises Inc
Class IHigh risk
DrugRecalled August 15, 2018
Montelukast Sodium Tablets 10 mg, 30-count bottle, Rx Only, By: Hetero Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, Manfuactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, NDC 31722-726-30
Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg tablets may contain 90 tablets of Losartan Potassium 50 mg.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- D-0081-2019
- Lot/product code:
- Lot #: MON17384, Exp 12/19
- Recalling firm:
- Hetero Labs Limited Unit V
Class IHigh risk
FoodRecalled October 4, 2018
Callie's Charleston Biscuits COUTRY HAM BISCUITS; 18 NET WT. 18 OZ (510 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM
The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes
AKALARAZCACOCTDCDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVOHOKORPARISCSDTNTXUTVAVTWAWIWVWY
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- F-0067-2019
- Lot/product code:
- 050417, 052417, 053017, 071017, 072417, 080117, 081417, 082217, 091417, 092717, 101017, 101117, 102417, 110617, 110817, 111417, 112017, 113017, 120817, 121117, 121417, 121817, 122217, 070219, 071519, 081319, 082619, 090819, 091519, 092619, 092719, 101019, 101619, 102319, 110119, 111119, 111419, 112919, 121319, 122119, 010920, 013020, 020620 & 031920.
- Recalling firm:
- Callie's Charleston Biscuits
Class IHigh risk
FoodRecalled October 4, 2018
Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM
The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes
AKALARAZCACOCTDCDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVOHOKORPARISCSDTNTXUTVAVTWAWIWVWY
▸Full report
The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- F-0066-2019
- Lot/product code:
- 050417, 060617, 060717, 080117, 091917, 092717, 110617, 120417, 121617, 070619, 080819, 101019, 102319, 110119, 111419, 122119 & 010920.
- Recalling firm:
- Callie's Charleston Biscuits
Class IHigh risk
FoodRecalled May 27, 2019
"DEEP***GOLDEN RAISINS***NET WT***198g/7oz***DEEP FOODS, INC. UNION, NJ 07083"
Deep Foods Inc., 1090 Springfield Road, Union, NJ-07083 is initiating a recall of Deep Golden Raisins because of not listed on the label sulfites.
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The most serious kind of recall. Using this product could cause serious health problems or death.
- Recall #:
- F-1981-2019
- Lot/product code:
- This recall covers 7oz, 14oz, and 28oz sizes with the following UPC codes: 7oz: 011433133432 14oz: 011433133449 28oz: 011433433457
- Recalling firm:
- Deep Foods Inc
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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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
A Clean Choice CBD, Hemp Oil Extract Tincture, Strawberry Creme, 1000mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Rd Suite 1, Saginaw, MI 48603
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-1455-2020
- Lot/product code:
- FG003108
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
Class IHigh risk
DrugRecalled June 18, 2020
Tasty Drops, Hemp Oil Extract, Vanilla, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29082 8
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-1476-2020
- Lot/product code:
- FG003140, FG003182, FG003246
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
Class IHigh risk
DrugRecalled June 18, 2020
Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Pathway to Wellness
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-1464-2020
- Lot/product code:
- FG003151
- Recalling firm:
- MICHIGAN HERBAL REMEDIES
Class IHigh risk
DrugRecalled June 18, 2020
BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Berry Blast, 500mg CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 146, Eau Claire, MI 49111
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-1457-2020
- Lot/product code:
- FG003312
- 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.
ALL 50 STATES
▸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 June 18, 2020
Goodness Gurus, Healthy Hemp Drops, 500MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 6 53341 99261 1
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-1461-2020
- Lot/product code:
- FG003234
- Recalling firm:
- MICHIGAN HERBAL REMEDIES