BIGNOPE
Ko-fi

Recalls affecting New Jersey

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

16,968 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 Mendietary 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 AliveMoringa 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. Braun0.9% 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 ValueOrganic 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

LipofitLipofit 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

KofinasGarlic 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 TemptationsChocolatey 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 SproutsRobust 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

MartinaMangoes

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)
Wording
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Paneer (bulk)

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0929-2024
Lot/product code:
PLU Batch ID 45845 B1-23284-Paneer 45845 B2-23284-Paneer 45845 B1-23298-Paneer 45845 B2-23298-Paneer 45845 B1-23311-Paneer 45845 B2-23311-Paneer 45845 B1-23333-Paneer 45845 B2-23333-Paneer 45845 B1-23345-Paneer 45845 B2-23345-Paneer 45845 B1-23354-Paneer 45845 B2-23354-Paneer 45845 B1-243-Paneer 45845 B2-243-Paneer 45845 B1-2418-Paneer 45845 B2-2418-Paneer
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Monterey Jack Conventional (bulk)

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0928-2024
Lot/product code:
PLU Batch ID 40200 1DZ-23249 40200 2DY-23249 40200 3DX-23249 40200 4CW-23249 40200 1DY-23279 40200 2DX-23279 40200 3CW-23279 40200 4CZ-23279 40200 1DZ-23283 40200 2DY-23283 40200 3CW-23283 40200 4CZ-23283 40200 2EY-23284 40200 3EX-23284 40200 4EW-23284 40200 1EX-23314 40200 2DW-23314 40200 3DZ-23314 40200 4DY-23314 40200 1DZ-24019 40200 2EY-24019 40200 3EX-24019 40200 4EW-24019 40200 1CY-24027 40200 2DX-24027 40200 3DW-24027 40200 4DZ-24027
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Tio Francisco Requeson 14 oz. UPC 7-27242-00390-6 Tio Francisco Requeson 15 oz. UPC 7-27242-00392-6 Tio Francisco Requeson Available to consumers at retail deli counters in various sizes

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0924-2024
Lot/product code:
All dates through 04/02/2024
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Tio Francisco Panela 14 oz. UPC 7-27242-00550-0 Food City Panela 16 oz. Tio Francisco, San Carlos, Dos Ranchitos, La Ordena, Campesino Panela Available to consumers at retail deli counters in various sizes Tio Francisco Panela Barra Available to consumers at retail deli counters in various sizes. Panela Regular and Barra (Bulk)

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0921-2024
Lot/product code:
All dates through 04/02/2024 Panela Regular and Barra (bulk) PLU Batch ID 12240 2C-23335 12350 2C-23335 12350 3C-23335 350 1C-23335 350 2C-23335 350 1B-23336 50350 3C-23338 26350 2C-23339 26350 3B-23339 350 1C-23339 350 2C-23339 50350 3B-23339 351 2AW-23340 350 2C-23340 351 4AW-23341 56351 4AW-23341 350 1C-23342 350 2C-23342 12240 3C-23345 12350 3C-23345 350 3C-23345 26350 2C-23346 350 1C-23346 350 2C-23346 350 3C-23346 50350 3C-23346 351 4AW-23347 351 3AW-23348 56351 3AW-23348 350 1C-23349 350 2D-23349 350 3D-23349 56350 1C-23349 12240 1C-23350 12350 1C-23350 350 2D-23350 350 3D-23350 350 3C-23352 26350 1C-23353 350 1C-23353 350 2C-23353 350 3C-23353 351 1AW-23354 12240 1C-23354 12350 1C-23354 50350 1C-23354 56350 1C-23354 351 3AW-23355 56351 3AW-23355 350 1B-23355 350 1B-23356 350 3C-23360 50350 3C-23360 26350 3C-23361 350 2C-23361 350 3C-23361 350 3C-23362 56350 3C-23362 351 3AW-23363 56351 3AW-23363 350 1B-23363 12240 1B-23364 12350 1B-23364 350 1B-23364 350 2D-23364 350 3D-23364 350 2C-24003 350 3C-24003 50350 1C-24003 56350 2C-24003 351 3AW-24004 351 3AW-24005 56351 3AW-24005 12240 2B-24006 12350 2B-24006 350 2B-24006 350 3B-24006 26350 1C-24008 350 2C-24008 350 3C-24008 350 2C-24010 350 3C-24010 351 4AW-24011 56351 4AW-24011 12240 2B-24012 12350 2B-24012 350 3B-24012 26350 3B-24015 350 2C-24015 350 3B-24015 56350 3B-24015 351 4AW-24018 351 4AW-24019 56351 4AW-24019 12240 2C-24020 12350 2C-24020 350 2C-24020 350 3C-24020 50350 2C-24020 26350 2C-24023 350 1C-24023 350 2C-24023 351 1AW-24026 12240 2C-24027 12350 2C-24027 350 2C-24027 350 1B-24029 26350 2C-24030 350 1D-24030 350 2C-24030 50350 3C-24030 56350 1D-24030 351 4AW-24031 350 1C-24032 350 2C-24032 12240 2C-24033 12350 2C-24033 350 1D-24033 350 2C-24033 350 3C-24033
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Tio Francisco Yogurt (Plain, Strawberry, Peach, Mango) Available to consumers at retail deli counters in various sizes

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0926-2024
Lot/product code:
All dates through 04/17/2024 PLU Batch ID 773 B1-23319-Stirred Yogurt Mango 771 B1-23319-Stirred Yogurt Peach 770 B1-23319-Stirred Yogurt Strawberry 773 B1-23333-Stirred Yogurt Mango 771 B1-23333-Stirred Yogurt Peach 770 B1-23333-Stirred Yogurt Strawberry 773 B1-23354-Stirred Yogurt Mango 771 B1-23354-Stirred Yogurt Peach 770 B1-23354-Stirred Yogurt Strawberry 773 B1-23362-Stirred Yogurt Mango 771 B1-23362-Stirred Yogurt Peach 770 B1-23362-Stirred Yogurt Strawberry 773 B1-2411-Stirred Yogurt Mango 771 B1-2411-Stirred Yogurt Peach 446 B1-2411-Stirred Yogurt Plain 770 B1-2411-Stirred Yogurt Strawberry 773 B1-2419-Stirred Yogurt Mango 771 B1-2419-Stirred Yogurt Peach 770 B1-2419-Stirred Yogurt Strawberry 773 B1-2432-Stirred Yogurt Mango 771 B1-2432-Stirred Yogurt Peach 446 B1-2432-Stirred Yogurt Plain 770 B1-2432-Stirred Yogurt Strawberry
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Tio Francisco Blanco Suave 14 oz. UPC 7-27242-05355-6

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0917-2024
Lot/product code:
All dates through 03/23/2024
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

365 Whole Foods Market Ricotta Part Skim 15 oz. UPC 9-94824-63052 365 Whole Foods Market Ricotta Whole Milk 15 oz. UPC 9-94824-96245 Ricotta Part Skim 65%, 70%, 75% Moisture (bulk)

Listeria monocytogenes contamination.

Full report

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

Recall #:
F-0925-2024
Lot/product code:
All dates through 04/02/2024 Ricotta (bulk) PLU Batch ID 390 B1-23338-Ricotta 65% Moisture 390 B2-23338-Ricotta 65% Moisture 366 B1-23338-Ricotta Part Skim 75% Moisture 366 B2-23338-Ricotta Part Skim 75% Moisture 366 B3-23338-Ricotta Part Skim 75% Moisture 366 B4-23338-Ricotta Part Skim 75% Moisture 366 B5-23338-Ricotta Part Skim 75% Moisture 366 B6-23338-Ricotta Part Skim 75% Moisture AK100047 B1-23339-Ricotta Part Skim 70% Moisture AK100047 B2-23339-Ricotta Part Skim 70% Moisture AK100047 B3-23339-Ricotta Part Skim 70% Moisture AK100047 B4-23339-Ricotta Part Skim 70% Moisture 366 B1-23339-Ricotta Part Skim 75% Moisture AK100047 B1-23340-Ricotta Part Skim 70% Moisture AK100047 B2-23340-Ricotta Part Skim 70% Moisture 366 B1-23340-Ricotta Part Skim 75% Moisture 390 B1-23345-Ricotta 65% Moisture 390 B1-23346-Ricotta 65% Moisture 39030 B1-23346-Ricotta 65% Moisture 39030 B2-23346-Ricotta 65% Moisture 390 B1-23347-Ricotta 65% Moisture 390 B2-23347-Ricotta 65% Moisture 390 B3-23347-Ricotta 65% Moisture 39030 B1-23347-Ricotta 65% Moisture 390 B1-23348-Ricotta 65% Moisture 390 B2-23348-Ricotta 65% Moisture 390 B1-23352-Ricotta 65% Moisture 390 B2-23352-Ricotta 65% Moisture 366 B1-23352-Ricotta Part Skim 75% Moisture 366 B2-23352-Ricotta Part Skim 75% Moisture 366 B3-23352-Ricotta Part Skim 75% Moisture 366 B4-23352-Ricotta Part Skim 75% Moisture 390 B1-23353-Ricotta 65% Moisture 390 B2-23353-Ricotta 65% Moisture 390 B3-23353-Ricotta 65% Moisture 390 B1-23354-Ricotta 65% Moisture 390 B2-23354-Ricotta 65% Moisture 366 B1-23354-Ricotta Part Skim 75% Moisture 366 B2-23354-Ricotta Part Skim 75% Moisture 366 B3-23354-Ricotta Part Skim 75% Moisture 390 B1-23355-Ricotta 65% Moisture 390 B2-23355-Ricotta 65% Moisture AK100105 B1-23360-Ricotta 65% Moisture AK100105 B2-23360-Ricotta 65% Moisture AK100105 B3-23360-Ricotta 65% Moisture AK100105 B4-23360-Ricotta 65% Moisture AK100047 B1-23361-Ricotta Part Skim 70% Moisture AK100047 B2-23361-Ricotta Part Skim 70% Moisture AK100047 B3-23361-Ricotta Part Skim 70% Moisture AK100047 B4-23361-Ricotta Part Skim 70% Moisture AK100047 B5-23361-Ricotta Part Skim 70% Moisture AK100047 B6-23361-Ricotta Part Skim 70% Moisture 390 B1-23363-Ricotta 65% Moisture 390 B2-23363-Ricotta 65% Moisture AK100047 B1-23363-Ricotta Part Skim 70% Moisture 390 B1-242-Ricotta 65% Moisture 39030 B1-242-Ricotta 65% Moisture 39030 B2-242-Ricotta 65% Moisture 39030 B3-242-Ricotta 65% Moisture 39030 B4-242-Ricotta 65% Moisture 390 B1-243-Ricotta 65% Moisture 390 B2-243-Ricotta 65% Moisture 390 B1-244-Ricotta 65% Moisture AK100105 B1-248-Ricotta 65% Moisture AK100105 B2-248-Ricotta 65% Moisture AK100105 B3-248-Ricotta 65% Moisture AK100105 B4-248-Ricotta 65% Moisture AK100105 B5-248-Ricotta 65% Moisture 366 B1-249-Ricotta Part Skim 75% Moisture 366 B2-249-Ricotta Part Skim 75% Moisture 366 B3-249-Ricotta Part Skim 75% Moisture 366 B4-249-Ricotta Part Skim 75% Moisture 366 B5-249-Ricotta Part Skim 75% Moisture 366 B6-249-Ricotta Part Skim 75% Moisture 366 B7-249-Ricotta Part Skim 75% Moisture 390 B1-2411-Ricotta 65% Moisture 390 B2-2411-Ricotta 65% Moisture AK100105 B1-2411-Ricotta 65% Moisture AK100105 B2-2411-Ricotta 65% Moisture 390 B1-2412-Ricotta 65% Moisture 390 B2-2412-Ricotta 65% Moisture AK100047 B1-2415-Ricotta Part Skim 70% Moisture AK100047 B2-2415-Ricotta Part Skim 70% Moisture AK100047 B3-2415-Ricotta Part Skim 70% Moisture AK100047 B4-2415-Ricotta Part Skim 70% Moisture AK100047 B5-2415-Ricotta Part Skim 70% Moisture AK100047 B6-2415-Ricotta Part Skim 70% Moisture AK100047 B7-2415-Ricotta Part Skim 70% Moisture 390 B1-2416-Ricotta 65% Moisture 390 B2-2416-Ricotta 65% Moisture 390 B3-2416-Ricotta 65% Moisture 390 B4-2416-Ricotta 65% Moisture AK100105 B1-2418-Ricotta 65% Moisture AK100105 B2-2418-Ricotta 65% Moisture AK100105 B1-2419-Ricotta 65% Moisture AK100105 B2-2419-Ricotta 65% Moisture AK100105 B3-2419-Ricotta 65% Moisture AK100105 B4-2419-Ricotta 65% Moisture 390 B1-2422-Ricotta 65% Moisture 390 B2-2422-Ricotta 65% Moisture 390 B3-2422-Ricotta 65% Moisture 390 B5-2422-Ricotta 65% Moisture 390 B6-2422-Ricotta 65% Moisture 390 B1-2423-Ricotta 65% Moisture 39030 B1-2423-Ricotta 65% Moisture 39030 B2-2423-Ricotta 65% Moisture 39030 B3-2423-Ricotta 65% Moisture 39030 B1-2424-Ricotta 65% Moisture AK100047 B1-2425-Ricotta Part Skim 70% Moisture AK100047 B2-2425-Ricotta Part Skim 70% Moisture AK100047 B3-2425-Ricotta Part Skim 70% Moisture 390 B1-2426-Ricotta 65% Moisture 390 B2-2426-Ricotta 65% Moisture 39030 B1-2426-Ricotta 65% Moisture AK100047 B1-2426-Ricotta Part Skim 70% Moisture AK100047 B2-2426-Ricotta Part Skim 70% Moisture AK100105 B1-2429-Ricotta 65% Moisture AK100105 B2-2429-Ricotta 65% Moisture AK100105 B3-2429-Ricotta 65% Moisture AK100105 B1-2430-Ricotta 65% Moisture AK100105 B2-2430-Ricotta 65% Moisture AK100105 B3-2430-Ricotta 65% Moisture AK100105 B4-2430-Ricotta 65% Moisture AK100105 B5-2430-Ricotta 65% Moisture 390 B1-2431-Ricotta 65% Moisture AK100105 B1-2431-Ricotta 65% Moisture … (truncated, 9118 characters total — see the official FDA record for the full value)
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL), Item F3360, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-148-94.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

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

Recall #:
D-0279-2024
Lot/product code:
Lot #: 2330993, Exp. Date 02/15/2024; 2331010, Exp. Date 02/10/2024; 2331055, Exp. Date 01/18/2024; 2331113, Exp. Date 02/26/2024; 2331181, Exp. Date 03/04/2024; 2331187, Exp. Date 03/23/2024; 2331266, Exp. Date 03/31/2024; 2331343, Exp. Date 04/01/2024; 2331349, Exp. Date 04/23/2024; 2331433, Exp. Date 05/05/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

FentaNYL citrate PF, 2500 mcg per 250 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3342, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-82.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

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

Recall #:
D-0278-2024
Lot/product code:
Lot #: 2330988, Exp. Date 01/31/2024; 2331058, Exp. Date 02/18/2024; 2331150, Exp. Date 03/10/2024; 2331231, Exp. Date 03/24/2024; 2331289, Exp. Date 03/30/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3208, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-029-68.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

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

Recall #:
D-0282-2024
Lot/product code:
Lot #: 2331140, Exp. Date 02/08/2024; 2331188, Exp. Date 02/15/2024; 2331261, Exp. Date 03/05/2024; 2331287, Exp. Date 03/14/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

FentaNYL citrate PF, 1000 mcg per 100 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3355, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-41.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

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

Recall #:
D-0277-2024
Lot/product code:
Lot #: 2331062, Exp. Date: 02/08/2024; 2331224, Exp. Date 03/18/2024; 2331270, Exp. Date 03/28/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-028-68.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

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

Recall #:
D-0281-2024
Lot/product code:
Lot #: 2331184, Exp. Date 02/13/2024; 2331185, Exp. Date 02/10/2024; 2331189, Exp. Date 02/20/2024; 2331191, Exp. Date 02/24/2024; 2331258,Exp. Date 03/03/2024; 2331317, Exp. Date 03/15/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL), Item F3352, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-150-82.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

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

Recall #:
D-0280-2024
Lot/product code:
Lot #: 2330939, Exp. Date 01/30/2024; 2331032, Exp. Date 02/03/2024; 2331112, Exp. Date 03/19/2024; 2331190, Exp. Date 03/26/2024; 2331429, Exp. Date 04/28/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 26, 2023

Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Microbial Contamination of Non-Sterile Products

ALL 50 STATES
Full report

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

Recall #:
D-0317-2024
Lot/product code:
Lot#: T08740, T08742, Exp 06/30/2026
Recalling firm:
Haleon US Holdings LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 26, 2023

Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Microbial Contamination of Non-Sterile Products

ALL 50 STATES
Full report

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

Recall #:
D-0316-2024
Lot/product code:
a) Lot#: T10810, Exp 10/31/2025 b) Lot#: T08730, T08731, T08732, T08733, Exp 05/31/2025; T10808, Exp 09/30/2025
Recalling firm:
Haleon US Holdings LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled December 21, 2023

Americaine, (benzocaine 20%) Benzocaine Topical Anesthetic Spray, Aerosol Can 2 oz (57 G), Dist. by Insight Pharmaceuticals Corp. Tarrytown, NY 10591, USA, A Prestige Consumer Healthcare company. Made in India. NDC 63736-378-02, Can UPC 3 63736 37882 0; Case UPC 1 03 63736 37882 7

Chemical Contamination: presence of benzene

ALL 50 STATES
Full report

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

Recall #:
D-0236-2024
Lot/product code:
Lot # 1A16420, exp. date 01/31/2025
Recalling firm:
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).

Presence of Particulate Matter; identified as glass

ALL 50 STATES
Full report

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

Recall #:
D-0234-2024
Lot/product code:
Lot HA7295, EXP 03/01/2025
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira, Inc., Lake Forest, IL 68045, NDC 61703-332-18

Presence of particulate matter: glass

ALL 50 STATES
Full report

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

Recall #:
D-0261-2024
Lot/product code:
Lot #: BL12206A, Exp date 06/30/2024
Recalling firm:
PFIZER
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake FOrest, IL 60045, NDC 0409-4911-11 (carton), 0409-4911-34 (case).

Presence of Particulate Matter; identified as glass

ALL 50 STATES
Full report

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

Recall #:
D-0235-2024
Lot/product code:
Lot GY2496, Exp 02/01/2025
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).

Presence of Particulate Matter; identified as glass

ALL 50 STATES
Full report

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

Recall #:
D-0233-2024
Lot/product code:
Lot GX1542, Exp. 01/01/2025
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled November 29, 2023

Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ

Marketed without an approved NDA/ANDA: Magnum XXL found to contain not listed on the label active pharmaceutical ingredient (API) - Sildenafil.

ALL 50 STATES
Full report

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

Recall #:
D-0206-2024
Lot/product code:
All Lots
Recalling firm:
Meta Herbal
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 22, 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-0144-2024
Lot/product code:
Lot #: FX001500, FX001582, Exp. 09/30/2024
Recalling firm:
Novartis Pharmaceuticals Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled November 22, 2023

TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.

Chemical Contamination; presence of benzene.

ALL 50 STATES
Full report

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

Recall #:
D-0151-2024
Lot/product code:
Lot #s: 0H88645, Exp 07/31/2024; 0B88345, Exp 02/29/2024.
Recalling firm:
Insight Pharmaceuticals Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 17, 2023

Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box, Rx Only, Manufactured by: InvaGen Pharmaceuticals, Inc., (a subsidiary of Cipla Ltd.), Hauppauge, NY, 11788, Manufactured for: Cipla USA, Inc., Warren, NJ 07059, NDC 69097-964-53

Defective Container: powder may leak out of the pouch

ALL 50 STATES
Full report

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

Recall #:
D-0220-2024
Lot/product code:
Lot #: NB301030, Exp. Date 03/31/2025
Recalling firm:
InvaGen Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 13, 2023

Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 70000-0090-1) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 70000-0090-2), Distributed by: Cardinal Health Dublin, Ohio 43017

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-0291-2024
Lot/product code:
All lots
Recalling firm:
Kilitch Healthcare India Limited
View official FDA record (opens in a new tab)