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Recalls affecting South Carolina

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

16,706 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
FoodAllergenUndeclaredRecalled October 20, 2022

Umami Everyday Savory Spice, 5 fl. oz. (148 mL) glass bottle, UPC 8-50000-72724-3, Co-Packed with Seed Ranch Flavor Co., Denver, CO 80216 Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
▸Full report

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

Recall #:
F-0175-2023
Lot/product code:
Lot Codes: 120122 062521
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled November 5, 2022

Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz. (3,785 ml.) jug, NDC 74943-125-28, Manufactured by B&B Blending, LLC, Northglenn, CO.

Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL BASED HAND SANITIZER isopropyl alcohol 75% v/v to contain methanol.

ALL 50 STATES
▸Full report

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

Recall #:
D-0066-2023
Lot/product code:
Lot: 133475
Recalling firm:
Adam's Polishes LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 30, 2023

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

ALL 50 STATES
▸Full report

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

Recall #:
D-0919-2023
Lot/product code:
Lot #: PCMI005, Exp. date AUG-2024; PCMJ001, PCMJ002, PCMJ004, PCMJ005, PCMJ006, PCMJ008, PCMJ009, PCMJ010, PCMJ011, PCMJ012, PCMJ013, PCMJ014, PCMJ015, Exp. date MAR-2025
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 30, 2023

Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

ALL 50 STATES
▸Full report

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

Recall #:
D-0921-2023
Lot/product code:
Lot #: PCMH001, PCMH002, PCMH005, PCMH007, Exp. date NOV-2023
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Strawberry Low Fat Yogurt, Fruit & Granola Parfait, Net Wt. 5.5 Oz. Single Serving, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

CTDCDEMAMDNCNJNYPASCVA
▸Full report

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

Recall #:
F-0507-2023
Lot/product code:
UPC Code : 813141020826
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, LOW FAT YOGURT, FRUIT & GRANOLA PARFAIT, Newt, WT 9.oz , Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

CTDCDEMAMDNCNJNYPASCVA
▸Full report

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

Recall #:
F-0457-2023
Lot/product code:
UPC Code : 813141021090
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Turkey Sausage, Egg & Cheddar Muffin Net Wt. 5.5 Oz. Single Serving, Mylar Wrap, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

CTDCDEMAMDNCNJNYPASCVA
▸Full report

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

Recall #:
F-0455-2023
Lot/product code:
UPC Code : 813141022103
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Egg, Cheddar & Swiss Ciabatta, Net Wt. 5.3 Oz. Single Serving, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

CTDCDEMAMDNCNJNYPASCVA
▸Full report

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

Recall #:
F-0477-2023
Lot/product code:
UPC Code : 813141020956
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Sausage Egg & Cheese Croissant Net Wt. 6.25 Oz. Single Serving, Mylar Wrap, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

CTDCDEMAMDNCNJNYPASCVA
▸Full report

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

Recall #:
F-0456-2023
Lot/product code:
UPC Code : 813141020925
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 14, 2023

Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.

Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.

ALL 50 STATES
▸Full report

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

Recall #:
D-0455-2023
Lot/product code:
All Lots
Recalling firm:
Nanomaterials Discovery Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 14, 2023

Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.

Non-Sterility

ALL 50 STATES
▸Full report

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

Recall #:
D-0456-2023
Lot/product code:
Lot #s: a) 1808051, Exp.: 01/01/2027; b) 2203PS01, Exp.: 01/01/2027
Recalling firm:
Pharmedica USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 24, 2023

Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.

Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.

ALL 50 STATES
▸Full report

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

Recall #:
D-0488-2023
Lot/product code:
Batch # H29, Exp. Date 11/30/2023
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 13, 2023

Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC# 31722-629-21.

Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.

ALL 50 STATES
▸Full report

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

Recall #:
D-0567-2023
Lot/product code:
Lot# E220182, Exp. 12/31/2023
Recalling firm:
Camber Pharmaceuticals Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 14, 2023

COLE SLAW Ingredients: cabbage, mayonaise sugar, vinegar, celery seed, salt WT 16 oz WASHINGTON CRAB Carolina seafood

Not listed on the label egg and soy.

NCSC
▸Full report

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

Recall #:
F-0928-2023
Lot/product code:
Sell by Date 11/4/22-4/14/23
Recalling firm:
Washington Crab & Seafood Company, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 14, 2023

CRABCAKE Ingredients: Blue Crabmeat, mayonnaise, onion bread crumbs, egg solids, salt, spices paprika WASHINGTON CRAB Carolina seafood

Not listed on the label egg, wheat and soy.

NCSC
▸Full report

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

Recall #:
F-0929-2023
Lot/product code:
2 ct & 6 ct packages with Sell by Dates between 11/4/22 - 4/25/23 12 ct packages with Julian dates between 27022 - 09423
Recalling firm:
Washington Crab & Seafood Company, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0571-2023
Lot/product code:
No lot number, Exp: 06/2026
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0573-2023
Lot/product code:
Lot/Item#: OMS760-B, Exp: 12/2025
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0572-2023
Lot/product code:
Lot#: RO 927996, Exp: 12/25/2024
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled June 30, 2023

BURGER BUN WITH SEEDS 3507402 Flour, water, potato flour, eggs, sugar, shortening, milk powder, salt, yeast, S200 UPC 682863 049657

The firm was notified that their labels do not list the allergens wheat and sesame.

SC
▸Full report

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

Recall #:
F-1399-2023
Lot/product code:
All codes up to and including Sell By SEPT 29 23
Recalling firm:
Saffron Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 3, 2023

Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-1150-2023
Lot/product code:
All lots, Expires: 01/31/2025
Recalling firm:
APG SEVEN, INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 26, 2023

Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, UPC 00854582001111.

Non-Sterility

ALL 50 STATES
▸Full report

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

Recall #:
D-0037-2024
Lot/product code:
Lot: 6786, Exp: 03/31/25
Recalling firm:
Dr. Berne's Whole Health Products
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled September 8, 2023

SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, NDC 0078-0110-22.

Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals.

ALL 50 STATES
▸Full report

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

Recall #:
D-1174-2023
Lot/product code:
FX001691, Exp. 12/31/2025
Recalling firm:
Novartis Pharmaceuticals Corp.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled September 8, 2023

TheraBreath for Kids! Oral Rinse, sodium fluoride 0.05% (0.02% w/v fluoride ion), 16 fl. oz. 473 mL bottles, Strawberry Splash, UPC 6 97029 70000 6, manufactured for Church & Dwight Co, Inc., Ewing, NJ 08628

Microbial contamination of Non-Sterile Product; presence of yeast identified as Candida parapsilosis

ALL 50 STATES
▸Full report

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

Recall #:
D-0046-2024
Lot/product code:
Lot # PA3083011, Exp 3/31/2025
Recalling firm:
Church & Dwight Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled September 25, 2023

BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04

Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial beta-lactam compound).

ALL 50 STATES
▸Full report

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

Recall #:
D-0042-2024
Lot/product code:
Lot# LF21000008, Exp. 11/30/2023 Lot# LF22000051, Exp. 11/30/2025
Recalling firm:
Scynexis, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 18, 2023

ELCYS (cysteine hydrochloride injection), USP, 500 mg/10mL (50 mg/mL), 10x10 mL Single Dose Sterile Vials, For Intravenous Infusion Only, Rx Only, Manufactured and Distributed by Exela Pharma Sciences, LLC, Lenoir, NC 28645, (Vial: NDC 51754-1007-1; Carton: 51754-1007-3).

Presence of Particulate Matter: Silicone

ALL 50 STATES
▸Full report

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

Recall #:
D-0118-2024
Lot/product code:
Lot # 10000798, Expiration Date 03/31/2025
Recalling firm:
Exela Pharma Sciences LLC
View official FDA record (opens in a new tab)