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Recalls affecting Iowa

Data last updated: September 6, 2026 at 10:21 PM UTC

16,432 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
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Wording
Class IHigh risk
FoodRecalled April 20, 2026

Low Heat Non-Fat Dried Milk Powder - paper bags 25 kg. (packed under 5 labels: Off Grade NFDM Variable; Extra Grade NFDM Standard rBST Free; Grade A NFDM LH Basic; Grade A NFDM LH Standard rBST Free; Grade A NFDM LH Tier 1 rBST Free)

Potential contamination with Salmonella.

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

Recall #:
H-0699-2026
Lot/product code:
Batch Codes for recalled product all start with A or B full list below. Batch Codes and Production Date: B22725-01-A 8/15/2025; B22725-01-B 8/15/2025; B22725-01-C 8/15/2025; B22725-01-D 8/15/2025; B22725-01-E 8/15/2025; B22725-01-F 8/15/2025; B22725-01-G 8/15/2025; B22725-01-H 8/15/2025; B22825-01-A 8/16/2025; B22825-01-B 8/16/2025; B22825-02-A 8/16/2025; B22825-02-B 8/16/2025; B22825-02-C 8/16/2025; B22825-02-D 8/16/2025; B22825-02-E 8/16/2025; B22825-02-F 8/16/2025; B22825-02-G 8/16/2025; B22825-02-H 8/16/2025; B22825-03-A 8/16/2025; B22825-03-B 8/16/2025; B22825-03-C 8/16/2025; B22825-03-D 8/16/2025; B22825-03-E 8/16/2025; B22825-03-F 8/16/2025; B22825-03-G 8/16/2025; B22825-03-H 8/16/2025; B22825-04-A 8/16/2025; B22825-04-B 8/16/2025; B22825-04-C 8/16/2025; B22825-04-D 8/16/2025; B22825-04-E 8/16/2025; B22825-04-F 8/16/2025; B22825-04-G 8/16/2025; B22825-04-H 8/16/2025; B22825-05-A 8/16/2025; B22825-05-B 8/16/2025; B22825-05-C 8/16/2025; B22825-05-D 8/16/2025; B22825-05-E 8/16/2025; B22825-05-F 8/16/2025; B22825-05-G 8/16/2025; B22825-05-H 8/16/2025; B22925-05-A 8/17/2025; B22925-05-B 8/17/2025; B22925-05-C 8/17/2025; B22925-05-D 8/17/2025; B22925-05-E 8/17/2025; B22925-05-F 8/17/2025; B22925-05-G 8/17/2025; B22925-05-H 8/17/2025; B22925-06-A 8/17/2025; B22925-06-B 8/17/2025; B22925-06-C 8/17/2025; B22925-06-D 8/17/2025; B22925-06-E 8/17/2025; B22925-06-F 8/17/2025; B22925-06-G 8/17/2025; B22925-06-H 8/17/2025; B23025-01-A 8/18/2025; B23025-01-B 8/18/2025; B23025-01-C 8/18/2025; B23025-01-D 8/18/2025; B23025-01-E 8/18/2025; B23025-01-F 8/18/2025; B23025-01-G 8/18/2025; B23025-01-H 8/18/2025; B23025-02-A 8/18/2025; B23025-02-B 8/18/2025; B23025-02-C 8/18/2025; B23025-02-D 8/18/2025; B23025-02-E 8/18/2025; B23025-02-F 8/18/2025; B23025-02-G 8/18/2025; B23025-02-H 8/18/2025; B23025-03-A 8/18/2025; B23025-03-B 8/18/2025; B23025-03-C 8/18/2025; B23025-03-D 8/18/2025; B23025-03-E 8/18/2025; B23025-03-F 8/18/2025; B23025-03-G 8/18/2025; B23025-03-H 8/18/2025; B23025-04-A 8/18/2025; B23025-04-B 8/18/2025; B23025-04-C 8/18/2025; B23025-04-D 8/18/2025; B23025-04-E 8/18/2025; B23025-04-F 8/18/2025; B23025-04-G 8/18/2025; B23025-04-H 8/18/2025; B23125-10-A 8/19/2025; B23125-10-B 8/19/2025; B23125-10-C 8/19/2025; B23125-10-D 8/19/2025; B23125-10-E 8/19/2025; B23125-10-F 8/19/2025; B23125-10-G 8/19/2025; B23125-10-H 8/19/2025; B23425-02-A 8/22/2025; B23425-02-B 8/22/2025; B23425-02-C 8/22/2025; B23425-02-D 8/22/2025; B23425-02-E 8/22/2025; B23425-02-F 8/22/2025; B23425-02-G 8/22/2025; B23425-02-H 8/22/2025; B23425-03-A 8/22/2025; B23425-03-B 8/22/2025; B23425-03-C 8/22/2025; B23425-03-D 8/22/2025; B23425-03-E 8/22/2025; B23425-03-F 8/22/2025; B23425-03-G 8/22/2025; B23425-03-H 8/22/2025; B23625-01-A 8/24/2025; B23625-01-B 8/24/2025; B23625-01-C 8/24/2025; B23625-01-D 8/24/2025; B23625-01-E 8/24/2025; B23625-01-F 8/24/2025; B23625-01-G 8/24/2025; B23625-01-H 8/24/2025; B23625-02-A 8/24/2025; B23625-02-B 8/24/2025; B23625-02-C 8/24/2025; B23625-02-D 8/24/2025; B23625-02-E 8/24/2025; B23625-02-F 8/24/2025; B23625-02-G 8/24/2025; B23625-02-H 8/24/2025; B23925-05-A 8/27/2025; B23925-05-B 8/27/2025; B23925-05-C 8/27/2025; B23925-05-D 8/27/2025; B23925-05-E 8/27/2025; B23925-05-F 8/27/2025; B23925-05-G 8/27/2025; B23925-05-H 8/27/2025; B23925-06-A 8/27/2025; B23925-06-B 8/27/2025; B23925-06-C 8/27/2025; B23925-06-D 8/27/2025; B23925-06-E 8/27/2025; B23925-06-F 8/27/2025; B23925-06-G 8/27/2025; B23925-06-H 8/27/2025; B24025-06-A 8/28/2025; B24025-06-B 8/28/2025; B24025-06-C 8/28/2025; B24025-06-D 8/28/2025; B24025-06-E 8/28/2025; B24025-06-F 8/28/2025; B24025-06-G 8/28/2025; B24025-06-H 8/28/2025; B24025-07-A 8/28/2025; B24025-07-B 8/28/2025; B24025-07-C 8/28/2025; B24025-07-D 8/28/2025; B24025-07-E 8/28/2025; B24025-07-F 8/28/2025; B24025-07-G 8/28/2025; B24025-07-H 8/28/2025; B24125-01-A 8/29/2025; B24125-01-B 8/29/2025; B24125-01-C 8/29/2025; B24125-01-D 8/29/2025; B24125-01-E 8/29/2025; B24125-01-F 8/29/2025; B24125-01-G 8/29/2025; B24125-01-H 8/29/2025; B24125-02-A 8/29/2025; B24125-02-B 8/29/2025; B24125-02-C 8/29/2025; B24125-02-D 8/29/2025; B24125-02-E 8/29/2025; B24125-02-F 8/29/2025; B24125-02-G 8/29/2025; B24125-02-H 8/29/2025; B24125-03-A 8/29/2025; B24125-03-B 8/29/2025; B24125-03-C 8/29/2025; B24125-03-D 8/29/2025; B24125-03-E 8/29/2025; B24125-03-F 8/29/2025; B24125-03-G 8/29/2025; B24125-03-H 8/29/2025; B24125-04-A 8/29/2025; B24125-04-B 8/29/2025; B24125-04-C 8/29/2025; B24125-04-D 8/29/2025; B24125-04-E 8/29/2025; B24125-04-F 8/29/2025; B24125-04-G 8/29/2025; B24125-04-H 8/29/2025; B24125-05-A 8/29/2025; B24125-05-B 8/29/2025; B24125-05-C 8/29/2025; B24125-05-D 8/29/2025; B24125-05-E 8/29/2025; B24125-05-F 8/29/2025; B24125-05-G 8/29/2025; B24125-05-H 8/29/2025; B24125-06-A 8/29/2025; B24125-06-B 8/29/2025; B24125-06-C 8/29/2025; B24125-06-D 8/29/2025; B24125-06-E 8/29/2025; B24125-06-F 8/29/2025; B24125-06-G 8/29/2025; B24125-06-H 8/29/2025; B24125-07-A 8/29/2025; B24125-07-B 8/29/2025; B24125-07-C 8… (truncated, 15041 characters total — see the official FDA record for the full value)
Recalling firm:
California Dairies Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 8, 2026

Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.

Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp

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

Recall #:
D-0692-2026
Lot/product code:
Lot#: BL3608, Exp. 07/01/28.
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 21, 2026

Kian Pee Wan Capsules, 30-count bottles

Marketed Without an Approved NDA/ANDA: Product contains not listed on the label drug ingredients dexamethasone and cyproheptadine.

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

Recall #:
D-0769-2026
Lot/product code:
All lots within expiry.
Recalling firm:
Buy-Herbal
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 18, 2026

Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad, 382110, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1720-3.

Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.

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

Recall #:
D-0478-2026
Lot/product code:
Lot: AH250162, Exp 8/31/2027
Recalling firm:
Amneal Pharmaceuticals, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 11, 2026

Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes

Salmonella spp. identified in finished product testing

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

Recall #:
H-0640-2026
Lot/product code:
NFDM Low Heat, NFDM High Heat, and SMP Medium Heat Lot Codes : 26015B; 26016B; 26017B; 26018B; 26019B; 26022B; 26023B; 26024B; 26024BT; 26025B; 26025BT; 26026B; 26027B; 26028B; 26029B; 26030B; 26034B; 26035B; 26040B; 26041B; 26041BT; 26042B; 26042BT; 26043B; 26044B; 26046BT; 26047BT; 26048BT. The products were packaged in 25 kg bags or 1 metric ton totes.
Recalling firm:
Lone Star Dairy Products LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 2, 2026

Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.

Non-Sterility: microbial contamination identified as Paenibacillus phoenicis

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

Recall #:
D-0528-2026
Lot/product code:
Lot #: 25H065362; 25J013962; 25J034762; 25J064562; 25K004962; 25K041262; 25K065062; 25L015362; 25H065462; 25J014062; 25J035762; 25J064762; 25K005062; 25K041362; 25K065162; 25L015462; 25H066062; 25J014862; 25J035862; 25J064862; 25K006162; 25K041462; 25K065262; 25L015662; 25H066162; 25J014962; 25J035962; 25J064962; 25K006262; 25K041562; 25K065362; 25L016362; 25H066262; 25J033962; 25J050362; 25J065762; 25K006362; 25K041662; 25K064562; 25L015962; 25H066362; 25J034862; 25J050462; 25J066262; 25K005162; 25K040462; 25K064662; 25L016062; 25H066462; 25J034062; 25J050562; 25J066362; 25K006462; 25K040562; 25K065462; 25L030162; 25J013462; 25J034162; 25J050962; 25K004062; 25K019662; 25K040662; 25K065562; 25L058062; 25J013562; 25J034262; 25J051062; 25K004162; 25K020862; 25K040762; 25K065662; 25M022362; 25J014362; 25J034362; 25J051262; 25K005262; 25K020962; 25K040962; 25K066262; 25M028462; 25J014462; 25J034462; 25J051362; 25J065962; 25K019762; 25K041062; 25K066162; 25H065962; 25J034962; 25J051462; 25J065062; 25K019862; 25K041162; 25K064862; 25H065762; 25J035062; 25J051762; 25J065162; 25K021062; 25K041762; 25K065862; 25H065862; 25J035162; 25J051862; 25J066062; 25K021162; 25K041862; 25K079962; 25H066862; 25J035262; 25J051962; 25J066162; 25K021262; 25K041962; 25K080962; 25H066962; 25J035362; 25J075762;25K004262; 25K019962; 25K042162; 25K081062; 25J013162; 25J013662; 25J051162; 25K004362; 25K020062; 25K042262; 25K080062; 25J013262; 25J014562; 25J052062; 25K004462; 25K021362; 25K040862; 25K080162; 25J013362; 25J014662; 25J052162; 25K004562; 25K021462; 25K042062; 25K080262; 25J014162; 25J014762; 25J052262; 25K004662; 25K021562; 25K063862; 25K080362; 25J014262; 25J034562; 25J052362; 25K005362; 25K020162; 25K020562; 25K080462; 25H065562; 25J034662; 25J064362; 25K005462; 25K020262; 25K020362; 25K081162; 25H065662; 25J035462; 25J064462; 25K005562; 25K020662; 25K020462; 25K081262; 25H066562; 25J035562; 25J064662; 25K005662; 25K021662; 25K021962; 25K081362; 25H066662; 25J035662; 25J065262; 25K005762; 25K021762; 25K022062; 25K081462; 25H066762;25J050662; 25J065362; 25K004762; 25K021862; 25K063962; 25K081562; 25J012962; 25J050762; 25J065462; 25K004862; 25K040062; 25K064062; 25K080562; 25J013062; 25J050862; 25J065562; 25K005862; 25K040162; 25K064162; 25L014062; 25J013762; 25J051562; 25J065662; 25K005962; 25K040262; 25K064262; 25L014162; 25J013862; 25J051662; 25J065862; 25K006062; 25K040362; 25K064462; 25L015262 within Expiry
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 13, 2026

Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement, take two (2) veggie capsules once a day. For best results, take 20-30 min before a meal with an 8oz. glass of water or as directed by your health professional; UPC: 8 60012 16172 0

Product may be contaminated with Salmonella

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

Recall #:
H-0546-2026
Lot/product code:
Lot # - Expiration Date: 5020591 - 03/2027 5020592 - 03/2027 5020593 - 03/2027 5020594 - 03/2027 5020595 - 03/2027 5020596 - 03/2027 5030246 - 04/2027 5030247 - 04/2027 5030248 - 04/2027 5030249 - 04/2027 5030250 - 04/2027 5030251 - 04/2027 5040270 - 05/2027 5040271 - 05/2027 5040272 - 05/2027 5040273 - 05/2027 5040274 - 05/2027 5040275 - 05/2027 5040276 - 05/2027 5040277 - 05/2027 5040278 - 05/2027 5040279 - 05/2027 5050053 - 6/2027 5050054 - 6/2027 5050055 - 6/2027 5050056 - 6/2027 5060069 - 07/2027 5060070 - 07/2027 5060071 - 07/2027 5060072 - 07/2027 5060073 - 07/2027 5060074 - 07/2027 5060075 - 07/2027 5060076 - 07/2027 5060077 - 07/2027 5060078 - 07/2027 5060079 - 07/2027 5060080 - 07/2027 5080084 - 9/2027 5080085 - 9/2027 5080086 - 9/2027 5090107 - 10/2027 5090108 - 10/2027 5090109 - 10/2027 5090113 - 10/2027 5090114 - 10/2027 5090115 - 10/2027 5090116 - 10/2027 5090117 - 10/2027 5090118 - 10/2027 5100039 - 11/2027 5100048 - 11/2027
Recalling firm:
Ambrosia Brands LLC
Resolved:
August 13, 2026
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 13, 2026

Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: White child-resistant plastic bottle with sticker label applied UPC 810057763779 (sometimes proceeded by 00)

A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

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

Recall #:
H-1108-2026
Lot/product code:
B#AAW.501.3; all expiration dates
Recalling firm:
Shaman Botanicals, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 13, 2026

Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724

A sample of the product had the active ingredient in a quantity greater than the labeled specification.

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

Recall #:
H-1107-2026
Lot/product code:
B#AAW.501.3; all expiration dates
Recalling firm:
Shaman Botanicals, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 28, 2026

Ashfiat Alharamain Energy Support 250ml/8fl. oz.

Not listed on the label tadalafil

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

Recall #:
H-1196-2026
Lot/product code:
Batch No: ENGOT24 EXP: OCT 2028 UPC: 1234561870003
Recalling firm:
AKKARCO LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 23, 2026

NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA). Product of Mexico/Argentina/Paraguay. Distributed by Navitas Organics Novato, CA USA 94949 UPC: 858847000284

Potential contamination with Salmonella.

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

Recall #:
H-0533-2026
Lot/product code:
W31025283 - Best If Used By: End APR 2027 W31025286 - Best If Used By: End APR 2027 W31025287 - Best If Used By: End APR 2027 W31025311 - Best If Used By: End MAY 2027 W31025314 - Best If Used By: End MAY 2027 W31025315 - Best If Used By: End MAY 2027 W31025316 - Best If Used By: End MAY 2027 W31025317 - Best If Used By: End MAY 2027
Recalling firm:
Navitas, LLC.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 16, 2026

UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate Drive, Suite 200, Raleigh, NC 27617, NDC 69448-025-63

Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.

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

Recall #:
D-0353-2026
Lot/product code:
Subset of Lot 2199821, Expires: 05/31/2027 Specific Serial Numbers being Recalled: 160R694TT06X; 1C74A686RPPG; 1W6A2M777N3V; 20825394KR8P; 242E2RK3EA92; 2DG49VH89EPG; 2WEA2ADK1P4H; 3KR2TVAG3VDH; 42M0V0G9PM84; 46E9XKDPTH1R; 4AM12WEAE48H; 4FGHR096DMNV; 4MWGWM991XNA; 4NEW8XD9DNM2; 4Y2PYDFN9YA1; 61EPX42R4K2A; 63FN9VW5CAV7; 69TG160DW2CV; 69XFP3TMTP7X; 6AWVDCNHTV61; 6CEFY72W5GPA; 6FHF1A59X0X4; 6GA64FNDVGXY; 6NW5FACPPWDW; 75V19CF2A0PA; 7HK7155YNAK3; 7R51VVA1WX9T; 7XCKXMH2EERC; 85D8MFVM66D4; 8F3Y5NFFHC64; 8RDWKPM53N5R; 8W1PVXC5NAFW; 9338DPED7P3R; 9A4CXFTGCPYN; 9FKN5NRDX99A; 9G79AR0RGAY4; 9K28G80GGYXN; 9NN7NXE40M13; A48PXEPE77YE; A8M168K58G64; AMR0RNWHTWMW; AR145NW8WTVX; AY19W6DEGRX4; C276HMDGRE49; CAY0ARAEGMCF; CKT370X2G4NP; D0DFAXCN6G5W; D54TXR8AD9Y8; DAK3XP1P3DMP; DH44AGKTX27F; E69E9K6C29VD; EK1D8P703RCH; EX947FYVW7Y6; F2K148YVNRDD; F4EVX8573F1V; FEXA7MENKWF1; FNDNMPAFH89D; G2W3WTMP5HK9; G5MN0F418FFY; G6XECANG6P01; G7FNVGWW3D72; GAHFFNX336GA; GKNTDP4AV6AA; GVPN5C4D23H6; GVPPYARK1FCD; GVXDAAA87GA1; GX7AP73W4HMH; HDTFT2W59K52; HDVG3W6VW59Y; HP703MKWGGM7; K8CGDV1301TP; KN6Y35T0A198; KVGC92YVC6XF; KYCP1Y7CK4R4; MEY2VW5MC0N9; MGH40F2679X3; N11XGETGDAVM; N9DGTY65NFGN; NH9VM1K2ECGP; NNCFT59RD1KF; NVFCXRWHX93N; P3XY0RNV0VPY; P609NH6W670V; P9Y7926YN82A; PA88CCXMWCMG; PKADTN18YR1X; PM0YHNNK6P4T; R11TYM5VE9CK; R45AXAEK4TTN; R6C3533P943P; RMW35MXX4R4K; RX75F9DA58W4; RXRCRP9272DG; RXTH041DMT5D; T2FW4C24F364; T442NHDFD7H8; TC3443DCR4F8; TK8TRR8NT92A; TT8K21TGYFWY; V255NE533X59; V6MYKEA7HN7P; V764DEYM4RYP; VCPTYV1EF0R1; VECGDTDV1Y3A; VEE09A07R9X5; VEER64AW2C51; VRN2TE3HPK5N; WF14WA03FNT2; WTP5TKRGNFGW; WWPMXV50FRM4; X1DKP0T2AE1W; X59C5AV3VDTG; XKG3T7811TD2; Y0CYY950EYK8; YCRW0EPK620Y; YNYA64T18DPW.
Recalling firm:
McKesson
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 15, 2026

Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.28oz (8g) STICKS - NET WT. 8.47oz (240g); Manufactured for Superfoods, Inc.; UPC: 850077468063

Products may be contaminated with Salmonella Typhimurium

ALL 50 STATES
▸Full report

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

Recall #:
H-0433-2026
Lot/product code:
The lot code is printed on the bottom back of the packaging in black and begins with the letter "A". Expiration dates from 08/2026 to 01/2028. 2024 Lots: AA24H013, A24I019, A24J012, A24J041, A24K019, A24L001, A24L013, A24L036, A24L035 2025 Lots: A25A009, A25A017, A25A018, A25B005, A25B004, A25C018, A25C022, A25D021, A25E005, A25E007, A25F019, A25G033, A25F029, A25G065, A25H005, A25H012, A25I005, A25I010, A25I032, A25J005, A25J028, A25J037, A25K007, A25K013, A25L006 Stick Pack Products: 32825-1, 34425-1
Recalling firm:
SUPERFOODS, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 15, 2026

a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 860013190811 b.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.32oz (9g) STICKS - NET WT. 9.52oz (270g); Manufactured for Superfoods, Inc.; UPC: 850077468070

Products may be contaminated with Salmonella Typhimurium

ALL 50 STATES
▸Full report

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

Recall #:
H-0434-2026
Lot/product code:
The lot code is printed on the bottom back of the packaging in black and begins with the letter "A". Expiration dates from 08/2026 to 01/2028. 2024 Lots: A24G012, A24I036, A24J005, A24J032, A24J037, A24K028, A24L014, A24L019, A24L032 2025 Lots: A25A005, A25A058, A25B006, A25D010, A25D036, A25D041, A25E008, A25F021, A25H009, A25H030, A25H045, A25I011, A25J036, A25K035 Stick Pack Products: 32925-1, 34525-1
Recalling firm:
SUPERFOODS, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a navy blue box, UPC 850055470002, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only). 2) Spring & Mulberry Pure Dark Minis Date-Sweetened Chocolate, Net Wt. 0.75 oz. (22g), individually packaged in a navy blue box, UPC 850055470132, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 64 bars (caddied)/204 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1103-2026
Lot/product code:
1) Pure Dark: Product Number SMBARPC20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025218 and Use By 02/28/2027 Batch/Lot 025219 and Use By 02/28/2027 Batch/Lot 025254 and Use By 03/31/2027 Batch/Lot 025266 and Use By 03/31/2027 Batch/Lot 025269 and Use By 03/31/2027 Batch/Lot 025324 and Use By 05/31/2027 Batch/Lot 025338 and Use By 06/30/2027 Batch/Lot 025350 and Use By 06/30/2027 2) Pure Dark Minis: Product Number SMBARPC30001 Batch/Lot 025273 and Use By 03/31/2027 Batch/Lot 025302 and Use By 04/30/2027 Batch/Lot 025303 and Use By 04/30/2027 Batch/Lot 026009 and Use By 07/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a burgundy box, UPC 850055470149, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination.

ALL 50 STATES
▸Full report

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

Recall #:
H-1101-2026
Lot/product code:
Product Number SMBARMF20001 Batch/Lot 025230 and Use By 02/28/2027 Batch/Lot 025287 and Use By 04/30/2027 Batch/Lot 025345 and Use By 06/30/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Modern Warrior Ready, Dietary Supplement, 60 CAPSULES

FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.

ALL 50 STATES
▸Full report

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

Recall #:
H-1178-2026
Lot/product code:
Product distributed between April of 2022 until December 8th of 2025.
Recalling firm:
Modern Warrior Life, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1097-2026
Lot/product code:
Product Number SMBARMB20001 Batch/Lot 025220 and Use By 08/31/2026 Batch/Lot 025223 and Use By 08/31/2026 Batch/Lot 025247 and Use By 09/30/2026 Batch/Lot 025248 and Use By 09/30/2026 Batch/Lot 025251 and Use By 09/30/2026 Batch/Lot 025253 and Use By 09/30/2026 Batch/Lot 025275 and Use By 10/31/2026 Batch/Lot 025281 and Use By 10/31/2026 Batch/Lot 025288 and Use By 10/31/2026 Batch/Lot 025296 and Use By 10/31/2026 Batch/Lot 025335 and Use By 12/31/2026 Batch/Lot 025337 and Use By 12/31/2026 Batch/Lot 026008 and Use By 01/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination.

ALL 50 STATES
▸Full report

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

Recall #:
H-1102-2026
Lot/product code:
Product Number SMBARPD20001 Batch/Lot 025233 and Use By 08/31/2026 Batch/Lot 025237 and Use By 08/31/2026 Batch/Lot 025238 and Use By 08/31/2026 Batch/Lot 025239 and Use By 08/31/2026 Batch/Lot 025240 and Use By 08/31/2026 Batch/Lot 025241 and Use By 08/31/2026 Batch/Lot 025261 and Use By 09/30/2026 Batch/Lot 025265 and Use By 09/30/2026 Batch/Lot 025267 and Use By 09/30/2026 Batch/Lot 025268 and Use By 09/30/2026 Batch/Lot 025290 and Use By 10/31/2026 Batch/Lot 025294 and Use By 10/31/2026 Batch/Lot 025329 and Use By 11/30/2026 Batch/Lot 025330 and Use By 11/30/2026 Batch/Lot 025339 and Use By 12/31/2026 Batch/Lot 025343 and Use By 12/31/2026
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1104-2026
Lot/product code:
Product Number SMBARSS20001 Batch/Lot 026013 and Use By 07/31/2027 Batch/Lot 026014 and Use By 07/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1096-2026
Lot/product code:
Product Number SMBARML20001 Batch/Lot 025225 and Use By 02/28/2027 Batch/Lot 025255 and Use By 03/31/2027 Batch/Lot 025272 and Use By 03/31/2027 Batch/Lot 025342 and Use By 06/30/2027 Batch/Lot 025364 and Use By 06/30/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Earl Grey Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470231, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1098-2026
Lot/product code:
Product Number SMBARBE20001 Batch/Lot 025258 and Use By 03/31/2027 Batch/Lot 025346 and Use By 06/30/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Coffee Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light brown box, UPC 850055470224, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1105-2026
Lot/product code:
Product Number SMBARCO20001 Batch/Lot 025226 and Use By 02/28/2027 Batch/Lot 025274 and Use By 04/30/2027 Batch/Lot 025344 and Use By 06/30/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1099-2026
Lot/product code:
Product Number SMBARLR20001 Batch/Lot 025204 and Use By 01/31/2027 Batch/Lot 025205 and Use By 01/31/2027 Batch/Lot 025212 and Use By 02/28/2027 Batch/Lot 025216 and Use By 02/28/2027 Batch/Lot 025259 and Use By 03/31/2027 Batch/Lot 025260 and Use By 03/31/2027 Batch/Lot 026037 and Use By 08/31/2027 Batch/Lot 026040 and Use By 08/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled January 9, 2026

Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

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

Recall #:
H-1106-2026
Lot/product code:
Product Number SMBARBO20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025289 and Use By 04/30/2027 Batch/Lot 025325 and Use By 05/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)