FDA Recall
TerminatedTerminated: June 4, 2024Historical recordClass II
Haloperidol Decanoate Injection, USP 100 mg/mL, 1 mL Single Dose Vials, Rx Only, Sterile, 10 Vials, Teva Pharmaceuticals, USA, Inc., North Wales, PA NDC 0703-7131-03
by Teva Pharmaceuticals USA
- Reason
- Lack of Assurance of Sterility
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 4, 2024Historical recordClass II
Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 2 mL Single-Use Vial, Rx Only, TEVA Parenteral Medicines, Inc. Irvine, CA 92618 NDC 0703-4502-04
by Teva Pharmaceuticals USA
- Reason
- Lack of Assurance of Sterility
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 4, 2024Historical recordClass II
Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, 10 mL Multiple Dose Vial, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-0045-01
by Teva Pharmaceuticals USA
- Reason
- Lack of Assurance of Sterility
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 4, 2024Historical recordClass II
Haloperidol Decanoate Injection, USP 50 mg/mL, 1 mL Single Dose Vials, Rx Only, Sterile, 10 Vials, Teva Pharmaceuticals, USA, Inc., North Wales, PA NDC 00703-7121-03
by Teva Pharmaceuticals USA
- Reason
- Lack of Assurance of Sterility
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 4, 2024Historical recordClass II
Leucovorin Calcium for Injection, equivalent to leucovorin 350 mg/vial (20 mg/mL), Rx Only, FOR IM or IV Use, Sterile, Teva Parenteral Medicines, Inc., Irvine, CA NDC 0703-5145-01; ALSO LABELED UNDER: NOVAPLUS, Manufactured By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-5145-91 (Novaplus, a registered trademark of Vizient, Inc.)
by Teva Pharmaceuticals USA
- Reason
- Lack of Assurance of Sterility
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 15, 2022Historical recordClass II
CONAGRA BRANDS
- Product
- Udi Gluten Free Double Chocolate Muffins, 10oz (284g) retail…
- Reason
- potential presence of an extraneous material (plastic)
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 15, 2022Historical recordClass II
CONAGRA BRANDS
- Product
- Udi Gluten Free Blueberry Muffins, 10oz (284g) retail contai…
- Reason
- potential presence of an extraneous material (plastic)
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 15, 2022Historical recordClass II
CONAGRA BRANDS
- Product
- Udi Gluten Free Chocolate Zucchini Muffins, 10oz retail cont…
- Reason
- potential presence of an extraneous material (plastic)
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 15, 2022Historical recordClass II
CONAGRA BRANDS
- Product
- Udi Gluten Free Banana Chocolate Chip Muffins, 10oz retail c…
- Reason
- potential presence of an extraneous material (plastic)
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 17, 2022Historical recordClass I
Forest Mushroom Food Inc.
- Product
- Guan's Enoki Mushroom; Champignon d'enoki 100 g/3.5 oz. and…
- Reason
- State of Massachusetts sampled Enoki Mushrooms and found them to be positive for Listeria monocytogenes.
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 31, 2022Historical recordClass II
bloommy Inc.
- Product
- "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN, JOIN…
- Reason
- Dietary supplement contains undeclared fish collagen
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 16, 2021Historical recordClass I
Simkins Brothers Sweets, LLC dba Natural Way Food Group
- Product
- Natural Way Almond Butter 16 oz. UPC 850001775175 packaged i…
- Reason
- Potential to contain undeclared peanuts
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 1, 2022Historical recordClass II
Pepsico Inc
- Product
- Evolve Vanilla Bean Plant-Based Protein Shake, 11oz "Tetra P…
- Reason
- undeclared soy
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 1, 2022Historical recordClass II
Pepsico Inc
- Product
- Evolve Double Chocolate Plant-Based Protein Shake, 11oz "Tet…
- Reason
- undeclared soy
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: August 12, 2024Historical recordClass III
NOW Health Group Inc.
- Product
- NOW 4x6 Acidophilus, 60 capsules per retail bottle. Item num…
- Reason
- Foreign capsules included in bottle. Undeclared ingredients.
- Published
- May 26, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 21, 2023Historical recordClass I
BD ChloraPrep Hi-Lite Orange 26 mL Applicator (2% w/v chlorhexidine gluconate (CHG) and 70% v/v Isopropyl alcohol (IPA)) Sterile Solution, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co, NDC 54365-400-38
by CareFusion 213, LLC
- Reason
- Defective Delivery System: An increase in complaints identified endcap being loose or falling off upon activation releasing glass shards containing the solution.
- Published
- May 19, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 27, 2023Historical recordClass II
Metformin HCl Extended-Release Tablets, USP, 500 mg, packaged in 500-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-142-02.
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Presence of foreign substance: identified as activated carbon.
- Published
- May 19, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 5, 2022Historical recordClass I
NATURE'S SUNSHINE PRODUCTS
- Product
- Love & Peas Protein Rich Meal Replacement, Sugar Free, 1 LB…
- Reason
- The firm was notified by an ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.
- Published
- May 19, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 5, 2022Historical recordClass I
NATURE'S SUNSHINE PRODUCTS
- Product
- Love & Peas Protein Rich Meal Replacement, 1 LB 8 OZ (675 G)…
- Reason
- The firm was notified by its ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.
- Published
- May 19, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Imperial Platinum 2000, 1 capsule, UPC 718122040702
by QMart
- Reason
- Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
- Published
- May 12, 2021
- 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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