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Recalls affecting Puerto Rico

Data last updated: September 6, 2026 at 11:49 PM UTC

16,123 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
Wording
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

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 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)
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 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

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 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

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 December 23, 2025

Spice Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags

Not listed on the label Milk Allergen

ALL 50 STATES
Full report

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

Recall #:
H-0499-2026
Lot/product code:
Batch 221
Recalling firm:
B.C. Williams Bakery Service, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 23, 2025

Swiss Chocolate Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags

Not listed on the label Milk Allergen

ALL 50 STATES
Full report

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

Recall #:
H-0501-2026
Lot/product code:
072925-220 and 071825-36
Recalling firm:
B.C. Williams Bakery Service, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 23, 2025

Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags

Not listed on the label Milk Allergen

ALL 50 STATES
Full report

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

Recall #:
H-0500-2026
Lot/product code:
Lot #072225-217 Lot #072225-218 Lot #080325-200 Lot #080325-201 Lot #081625-203 Lot #081625-204 Lot #092225-222 Lot #092225-223 Lot #092225-224 Lot #092225-225 Lot #092225-226 Lot #092225-227 Lot #092225-228 Lot #101725-208 Lot #101725-209
Recalling firm:
B.C. Williams Bakery Service, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 15, 2025

MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of not listed on the label sildenafil and tadalafil

ALL 50 STATES
Full report

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

Recall #:
D-0397-2026
Lot/product code:
All codes; Exp 12/31/2029
Recalling firm:
StuffbyNainax
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 12, 2025

ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

ALL 50 STATES
Full report

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

Recall #:
D-0288-2026
Lot/product code:
All lots within expiry.
Recalling firm:
Medinatura New Mexico, inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 12, 2025

ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

ALL 50 STATES
Full report

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

Recall #:
D-0289-2026
Lot/product code:
All lots within expiry.
Recalling firm:
Medinatura New Mexico, inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled December 8, 2025

Sam Dry Fruits & Nuts PISTACHIO Meats Whole LOT #: PK00459 NET WEIGHT: 30 LBS PACK DATE: AUGUST/2025 EXPIRATION DATE: AUGUST/2027

Potential contamination with Salmonella.

ALL 50 STATES
Full report

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

Recall #:
H-0357-2026
Lot/product code:
LOT #: PK00459
Recalling firm:
Sam Dry Fruits and Nuts Enterprises, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled November 8, 2025

1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets

Contaminated with Clostridium botulinum

ALL 50 STATES
Full report

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

Recall #:
H-0249-2026
Lot/product code:
All batches and codes within expiry Finished Product Quantity 08NOV2023 to 08NOV2025 UPC Codes: Single Can: 8 50044 96800 8; Sams Club 2PK: 00850044968893; Amazon 2PK: 00850044968053; Anywhere pack: 8 50044 96802 2; 1-Count Sample Unit Anywhere Pack: 850044968015
Recalling firm:
ByHeart, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 6, 2025

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

ALL 50 STATES
Full report

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

Recall #:
D-0182-2026
Lot/product code:
Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 29, 2025

POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14

Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq

ALL 50 STATES
Full report

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

Recall #:
D-0180-2026
Lot/product code:
Lot # 1030613, Exp Date: 09/30/2026
Recalling firm:
Otsuka ICU Medical LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 29, 2025

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26

Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq

ALL 50 STATES
Full report

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

Recall #:
D-0181-2026
Lot/product code:
Lot # 1030613, Exp Date: 09/30/2026
Recalling firm:
Otsuka ICU Medical LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 24, 2025

Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775

Potential contamination of Salmonella Richmond

ALL 50 STATES
Full report

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

Recall #:
H-0205-2026
Lot/product code:
500-00055034; 500-00055035; 500-00055036; 500-00055037; 500-00055038; 500-00055039 500-00055040; 500-00055042; 500-00055043; 500-00055044; 500-00055045; 500-00055046 500-00055047; 500-00055048; 500-00055049; 500-00055050; 500-00055051; 500-00055052 500-00055053; 500-00055054; 500-00055055; 500-00055056; 500-00055057; 500-00055058 500-00056121; 500-00056122; 500-00056123; 500-00056124; 500-00056125; 500-00056126 500-00056127; 500-00056128; 500-00056129; 500-00056130; 500-00056131; 500-00056132 500-00056133; 500-00056134; 500-00056135; 500-00056136; 500-00056137; 500-00056138 500-00056139; 500-00056140; 500-00056141; 500-00056142; 500-00056143; 500-00056144 500-00056145; 500-00056146; 500-00056147; 500-00056148; 500-00056149; 500-00056150 500-00056151; 500-00056152; 500-00056153; 500-00056154; 500-00056155; 500-00056230 500-00056231; 500-00056318; 500-00056323; 500-00056429; 500-00056772;
Recalling firm:
MeriCal, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 20, 2025

SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of not listed on the label meloxicam.

ALL 50 STATES
Full report

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

Recall #:
D-0388-2026
Lot/product code:
All lots within expiry
Recalling firm:
ANTHONY TRINH, 123Herbals LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 8, 2025

Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0

Marketed Without an Approved NDA/ANDA-FDA analysis revealed not listed on the label sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).

ALL 50 STATES
Full report

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

Recall #:
D-0396-2026
Lot/product code:
ALL LOTS, exp 12/31/2027
Recalling firm:
Mohamed Hagar
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled September 16, 2025

Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1

Weaker than it should be Drug: Testing revealed there was no oxytocin in the IV bag.

ALL 50 STATES
Full report

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

Recall #:
D-0015-2026
Lot/product code:
Lot #: 20250620OXY-1, Expiration date 10/18/2025
Recalling firm:
IntegraDose Compounding Services LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 28, 2025

Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660

Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil

ALL 50 STATES
Full report

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

Recall #:
D-0304-2026
Lot/product code:
LOT308EXP03/28
Recalling firm:
Green Lumber Holdings, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 27, 2025

Cyclobenzaprine Hydrochloride Tablets, USP, 10 mg, 90-count bottle, RX only, Manufactured by: Unichem Laboratories, Ltd, Pilerne Ind. Estate, Pilerne, Bardez, Goa, India; Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ. NDC 29300-415-19.

Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).

ALL 50 STATES
Full report

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

Recall #:
D-0655-2025
Lot/product code:
Lot No: GMML24026A, Expires: 09/30/2027
Recalling firm:
Unichem Pharmaceuticals USA Inc.
View official FDA record (opens in a new tab)