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Recalls affecting Idaho

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

16,282 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
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Face Neck Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-167
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Lima Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-927
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 670-056, 681-014
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Tummy Tuck Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-223
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Stradi 4500 - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-1102
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Suction Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 670-057
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Face Lift Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-102
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-949, 682-937, 682-900, 682-370, 682-218, 682-1264, 682-1529, 682-076, 682-192, 682-962, 682-968, 682-177, 682-394, 682-988, 682-156, 682-063, 682-151, 682-917, 682-250, 682-409, 682-960, 682-945, 682-218, 682-1264, 682-1412, 682-1422
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

General Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 670-115
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Mississippi Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-1302
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

ACL Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-055
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Basic Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-203, 888-2375, 888-2396, 888-2430, 888-2495, 888-2594
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Vein & Vascular Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-670
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Glaucoma Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 687-395
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Laser Evlt Pack and Laser One Leg Evlt - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-670, 682-501, 682-547
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Lipo/Buttocks Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 681-256
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Plastic Pack and Plastic HNP Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-210, 693-054, 693-219, 888-2479, 888-2499
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

ENT Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2352, 888-2434
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Phleb Pack and Laser Phleb Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-1284, 682-299, 682-410, 682-353, 682-377, 682-548
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Breast Augmentation Pack and Breast Augmentation Expanded Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 681-502, 693-177, 681-243, 681-502, 681-502, 693-158, 682-502, 681-503
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Hand Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 693-057, 888-2345, 888-2596
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Hand Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2376, 888-2397, 888-2414, 888-2471
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Surgical Pack and General Surgery Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 40604EBS, 693-152, 40759MMS, 888-2371
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Skin and Vein Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-1218
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Advanced Vein Care - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
▸Full report

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

Recall #:
71130
Lot/product code:
Pack 682-956
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)