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Recalls affecting Nevada

Data last updated: September 8, 2026 at 1:13 PM UTC

16,567 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

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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

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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

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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

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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 IIModerate risk
DrugRecalled April 24, 2019

Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Dose Rx Only NDC 50268-517-15 Manufactured for: AvKARE Inc. Pulaski, TN 38478

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 0.96 parts per million.

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1249-2019
Lot/product code:
Lot: 20121 Exp. 6/30/2019
Recalling firm:
AVKARE Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 25, 2019

Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access

Failure to comply event due to incorrect labeling of a class 1 laser product.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
83302
Lot/product code:
Model: L1, identified by Accession No. RH19A0069
Recalling firm:
ASTRA, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 907734
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 903530
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 905617, 905618, 905619, 905620, 907004, 907005
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 905659, 905660, 906343
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 902108
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle Item code: 8881200029

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 904956
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 905657, 906327, 906341
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 904219, 904220, 907710
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 905611
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 904218, 904918, 906329
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 907007
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 902110, 902111
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 909117
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number:904212, 905612, 907002
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 905662
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 904901
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82927
Lot/product code:
Lot Number: 905613
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 3, 2019

Monarch Medical Technologies EndoTool IV, Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10.

Insulin dosing calculations were erroneously high.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82828
Lot/product code:
Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10
Recalling firm:
Monarch Medical Technologies
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 9, 2019

Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolidation has taken place. After this, the implant has no more use and can be removed.

The titanium implant has the wrong article number laser marked on it.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82796
Lot/product code:
Model Number: 21206-10; Lot Code: 26/F42778
Recalling firm:
I.T.S. GmbH
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 15, 2019

InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application (app) is intended for use with the HH90 Handset and TM90 Communicator to program, adjust, and troubleshoot the Medtronic Models 3023 and 3058 InterStim neurostimulators for sacral neuromodulation therapy. The clinician uses the Clinician app to program settings for the patient. The A510 Clinician app, HH90 Handset, TM90 Communicator along with the A520 Patient app are only sold as a kit (TH90).

There is a potential for an unexpected increase in stimulation during InterStim programming with the A10 Clinician Application (on Medtronic's smart programmer).

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82626
Lot/product code:
Model Numbers/UDI: a) TH90G01/00763000058005  b) TH90GFA/00763000187231 c) TH90G02/00763000192259, 00763000192266, 00763000192273,  00763000192280, 00763000192297, 00763000192303, 00763000192310 d) TH90G03/00763000192310  ALL LOT/SERIAL NUMBERS
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82950
Lot/product code:
N6B0079KX N8A0029KX
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA 45 ARTICULATING XTRA THICK SULU, Item Code EGIA45AXT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82950
Lot/product code:
N6B0080KX N6C0975KX
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA45 CT AR MD THK REL, EGIA45CTAMT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
82950
Lot/product code:
N8L0401KY
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)