FDA Recall
🇺🇸 United States
TerminatedTerminated: September 26, 2024Historical recordClass III
Lidl US TRADING
- Product
- Banana Pepper Rings 16 FL OZ (1PT) 473ml UPC:4056489223863.…
- Reason
- Container integrity issued (punctured lid)
- Published
- March 20, 2024
- Distribution
- Distributed to distribution centers and…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 21, 2025Historical recordClass II
House of Coffee Beans, Inc
- Product
- Coffee 5 pound bags, 2 pound bags, 1 pound bags, 12 ounce ba…
- Reason
- potential allergen contact with almonds, pecans and coconut.
- Published
- March 20, 2024
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: February 5, 2026Historical recordClass III
Mercaptopurine Tablets, USP 50 mg, packaged in: a) 25-count bottle (NDC 69076-913-02), b) 250-count bottle (NDC 69076-913-25), Rx only, Manufactured for: Quinn Pharmaceuticals, Boca Raton, FL, www.quinnrx.com
by Stason Pharmaceuticals, Inc.
- Reason
- Failed Dissolution Specifications: results slightly under spec at at 9-months.
- Published
- March 13, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass III
Clindamycin Phosphate Topical Solution USP, 1%, 60 mL bottle, Manufactured for: Glasshouse Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, L5N 6R8, NDC 71428-0003-60
by Contract Pharmaceuticals Limited Canada
- Reason
- Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
- Published
- March 13, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass III
Clindamycin Phosphate, Topical Solution USP, 1%, 60 mL, Rx Only, Manufactured for and Distributed by: Marlex Pharmaceuticals, Inc., New Castle, DE 19720, NDC 10135-0691-61
by Contract Pharmaceuticals Limited Canada
- Reason
- Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
- Published
- March 13, 2024
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 4, 2025Historical recordClass I
Summer Fresh Salads Inc
- Product
- Wegmans Harissa Hummus Topped With Harrisa 10.5 ounce (298 g…
- Reason
- Product contains undeclared sesame.
- Published
- March 13, 2024
- Distribution
- Washington D.C., Delaware, Maryland, Mas…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 16, 2024Historical recordClass I
T Marzetti Co
- Product
- Chick-fil-a Polynesian Sauce Cup: 28g single serve food serv…
- Reason
- Undeclared Allergens - Wheat and Soy
- Published
- March 13, 2024
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 16, 2024Historical recordClass II
FGP Manufacturing, LLC
- Product
- Frios Gourmet Pops - Fruity Pebbles Popsicle 3oz frozen pops…
- Reason
- Undeclared Color Additives - Yellow #5
- Published
- March 13, 2024
- Distribution
- Distribution States: FL, OK, OH, SC, TX,…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 16, 2024Historical recordClass II
FGP Manufacturing, LLC
- Product
- Frios Gourmet Pops - Creamy Coconut Popsicle 3oz frozen pops…
- Reason
- Undeclared sulfites
- Published
- March 13, 2024
- Distribution
- Distribution States: FL, OK, OH, SC, TX,…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 16, 2024Historical recordClass I
FGP Manufacturing, LLC
- Product
- Frios Gourmet Pops - Banana Pudding Popsicle 3oz frozen pops…
- Reason
- Undeclared Allergens - Egg
- Published
- March 13, 2024
- Distribution
- Distribution States: FL, OK, OH, SC, TX,…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 5, 2025Historical recordClass I
Taylor Fresh Foods Inc
- Product
- COLD CASE, ROASTED STREET CORN SALAD 1/4.78# (KR) Separate K…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- March 13, 2024
- Distribution
- U.S. distribution to the following: AL,…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 5, 2025Historical recordClass IFDA Announcement
Taylor Fresh Foods Inc
- Product
- Marketside Bacon Ranch Crunch Chopped Salad Kit 12.76oz UPC…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- March 13, 2024
- Distribution
- U.S. distribution to the following: AL,…
- Announced by FDA
- February 9, 2024
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 19, 2025Historical recordClass I
TRUONG GIANG WAREHOUSE
- Product
- Golden Owl Dried Mango 7 oz (200g) UPC 816710-024461. Packag…
- Reason
- Undeclared sulfites
- Published
- March 13, 2024
- Distribution
- Distributed to FL, GA, IL, MA, MI, MN, M…
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FDA Recall
OngoingHistorical recordClass II
Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42
by Denver Solutions, LLC DBA Leiters Health
- Reason
- Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Moxifloxacin 5mg/ml, 1 ml in a Single- Dose Vial, Rx Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-097-42
by Denver Solutions, LLC DBA Leiters Health
- Reason
- Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42
by Denver Solutions, LLC DBA Leiters Health
- Reason
- Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: August 15, 2025Historical recordClass II
PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471
by Seatex LLC
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: August 15, 2025Historical recordClass II
7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033
by Seatex LLC
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: August 15, 2025Historical recordClass II
7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 330 Gal. cases, Distributed by: Magnus, 16005 Gateway Drive, Suite 300, Frisco, TX 75033
by Seatex LLC
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: August 15, 2025Historical recordClass II
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
by Seatex LLC
- Reason
- CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Published
- March 6, 2024
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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