FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Caesar Lite" (salad product) packed in 9.8oz. packages
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Caesar Bacon" (salad product) packed in 9.9oz., 10.3oz., an…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Caesar" (salad product) packed in 9.8oz., 10.5oz., 11.3oz.,…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Bacon Thousand Island" (salad product) packed in 9.4oz. pac…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Bacon & Blue" (salad product) packed in 10.8oz. and 10.9oz.…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Baby Spinach" (salad product) packed in 5oz., 6oz., 10oz.,…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Baby Kale" (salad product) packed in 5oz. packages
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Baby Greens" (salad product) packed in 6oz. packages
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Avocado Ranch" (salad product) packed in 9.7oz. and 12.8oz.…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Asian Avocado" (salad product) packed in 9.7oz. packages
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "Angel Hair" (salad product) packed in 10oz. packages
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "American" (salad product) packed in 11oz. and 24oz. package…
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 17, 2023Historical recordClass I
Fresh Express Inc (Div of Chiquita Brands)
- Product
- "5- Lettuce Mix" (salad product) packed in 6oz. packages
- Reason
- potential to be contaminated with Listeria monocytogenes
- Published
- February 2, 2022
- Distribution
- Products were distributed to 110 domesti…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 28, 2023Historical recordClass II
World Health Products LLC
- Product
- GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN;…
- Reason
- Product may contain undeclared milk.
- Published
- February 2, 2022
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, DE, FL…
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FDA Recall
TerminatedTerminated: June 21, 2023Historical recordClass II
Medique Pain-Off (Acetaminophen 250 mg, Aspirin (NSAID*) 250 mg, Caffeine 65 mg) Tablets, packaged in 2-count Tablets per Unit Dose Packet, packaged as a) 200-count Tablets (100 x 2) Unit Dose packets per carton, UPC 3 47682 22847 7, Reorder #22847; b) 500-count Tablets (250 x 2) Unit Dose packets per carton, UPC 3 47682 22813 2, Reorder #22813; c) 100-count Tablets (50 x 2) Unit Dose packets per carton, UPC 3 47682 22833 0, Reorder #22833; d) 24-count Tablets (12 x 2) Unit Dose packets per carton, UPC 3 47682 22864 4, Reorder #22864; Manufactured for Medique Products, Fort Myers, FL 33967.
by Medique Products
- Reason
- CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
- Published
- January 26, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: December 13, 2024Historical recordClass II
Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-058-04
by VistaPharm, Inc.
- Reason
- Failed Stability Specifications
- Published
- January 26, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: January 12, 2024Historical recordClass I
Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled Pens per carton (NDC 49502-0196-75), Rx only, Manufactured in Malaysia for: Mylan Specialty L.P., Morgantown, WV, 26505.
by MYLAN PHARMACEUTICALS INC
- Reason
- Labeling: Missing Label: label missing from some Semglee prefilled pens.
- Published
- January 26, 2022
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: June 21, 2023Historical recordClass II
Extra Strength Headache (acetaminophen 250 mg, aspirin 250 mg, caffeine 65 mg) tablets, packaged in 2-count tablets per packet, Manufactured for: Lil' Drug Store Products, Inc., Cedar Rapids, IA 52404
by Medique Products
- Reason
- CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
- Published
- January 26, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 21, 2023Historical recordClass II
Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg, 250 mg, 65 mg, packaged as 100-count Tablets (50 Packets, 2 tablets each) per carton, Manufactured for: Acme United Corporation 55 Walls Dr, Fairfield, CT 06824, UPC 0 73577 90316 6
by Medique Products
- Reason
- CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
- Published
- January 26, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: March 29, 2024Historical recordClass III
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
by Dr. Reddy's Laboratories, Inc.
- Reason
- Subpotent drug
- Published
- January 26, 2022
- 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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