FDA Recall
🇺🇸 United States
TerminatedTerminated: March 31, 2021Historical recordClass II
Rong Shing Trading Inc.
- Product
- GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard…
- Reason
- Product contains undeclared milk
- Published
- November 6, 2019
- Distribution
- Retailer in 7 states: KY, MD, NY, UT, VA…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 11, 2020Historical recordClass I
Super World Trading Inc.
- Product
- Dried Date NET WT: 12 oz(340g+/-5g) packed in clear plastic…
- Reason
- Product contains undeclared sulfites.
- Published
- November 6, 2019
- Distribution
- Product distributed in FL, GA, TX, MD
View recall →
FDA Recall
TerminatedTerminated: December 4, 2019Historical recordClass II
Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20
by Avella of Deer Valley, Inc. Store 38
- Reason
- Lack of sterility assurance.
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 1, 2020Historical recordClass II
del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10
by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- Reason
- Lack of Assurance of Sterility; bags have potential to leak
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 1, 2020Historical recordClass II
Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysine HCl, Single Dose Container, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-988-10
by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- Reason
- Lack of Assurance of Sterility; bags have potential to leak
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 1, 2020Historical recordClass II
PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Sodium Chloride Injection-200 mL Total Dose: (400 mcg/200 mg)/200 mL, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-526-20
by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- Reason
- GMP Deviations: potential glass contamination
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 1, 2020Historical recordClass II
PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride Injection-250 mL, Rx Only Total Dose: (500 mcg/312.5 mg)/250 mL, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-530-25
by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- Reason
- GMP Deviations: potential glass contamination
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 1, 2020Historical recordClass II
PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Sodium Chloride Injection-250 mL Total Dose: (500 mcg/156.3 mg)/250 mL, Rx Only, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC 69374-0525-25
by Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- Reason
- GMP Deviations: potential glass contamination
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: May 14, 2020Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo and Fresh Grab Ham & Cheese wheat sandwich, 5 oz., wit…
- Reason
- Products contain chicken which has been recalled by supplier because it may be contaminated with Listeria monocytogenes
- Published
- October 30, 2019
- Distribution
- The product was distributed to food serv…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: May 14, 2020Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo Signature Cranberry Almond Chicken Salad croissant san…
- Reason
- Products contain chicken which has been recalled by supplier because it may be contaminated with Listeria monocytogenes
- Published
- October 30, 2019
- Distribution
- The product was distributed to food serv…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: May 14, 2020Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz.,…
- Reason
- Products contain chicken which has been recalled by supplier because it may be contaminated with Listeria monocytogenes
- Published
- October 30, 2019
- Distribution
- The product was distributed to food serv…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 3, 2020Historical recordClass III
Threshold Enterprises Ltd
- Product
- Source Naturals Dietary Supplement Brain Charge Advanced…
- Reason
- Labeling error; incorrect supplement facts panel and label claims for two ingredients were lower than the product formulation.
- Published
- October 30, 2019
- Distribution
- U.S. distribution to the following: AL,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 28, 2020Historical recordClass I
Roland Foods, LLC
- Product
- Roland Brand Red Caviar - Whole Grain Lumpfish (Lumpfish Roe…
- Reason
- Potential to be contaminated with Clostridium botulinum.
- Published
- October 30, 2019
- Distribution
- Products were distributed in US states:…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 28, 2020Historical recordClass I
Roland Foods, LLC
- Product
- Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish R…
- Reason
- Potential to be contaminated with Clostridium botulinum.
- Published
- October 30, 2019
- Distribution
- Products were distributed in US states:…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 21, 2021Historical recordClass II
The Truck Farm, LLC
- Product
- Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix.…
- Reason
- The product contains wheat flour, but does not declare wheat on the label.
- Published
- October 30, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 1, 2020Historical recordClass II
Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus Pharmaceuticals, LLC. Orlando, FL 32839
by Ingenus Pharmaceuticals Llc
- Reason
- Crystallization: Presence of particulate matter identified as API crystallization
- Published
- October 23, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 4, 2023Historical recordClass II
Dextroamphetamine Sacharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, Mixed Salts of a single Entity Amphetamine Product), 20mg, 100-count bottle, RX Only, Distributed by: Aurobindo Pharma USA Inc., Dayton, NJ 08810, NDC 13107-073-01
by Aurobindo Pharma USA Inc.
- Reason
- Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of specification for weight and thickness.
- Published
- October 23, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 20, 2020Historical recordClass III
Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.
by KVK-Tech, Inc.
- Reason
- Presence of Foreign Substance; Fiber particles.
- Published
- October 23, 2019
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: November 10, 2020Historical recordClass II
Fentanyl Citrate USP, Active Pharmaceutical Ingredient, Spectrum Chemical MFG. CORP., Gardena, CA 90248 NDC 49452-0032-06
by Spectrum Laboratory Products
- Reason
- CGMP Deviations: Received notice from supplier that there is potential glass contamination.
- Published
- October 23, 2019
- Distribution
- Product was distributed to compounding p…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 10, 2020Historical recordClass I
E.A. Sween Co.
- Product
- Market Sandwich Artisan Style Albacore Tuna Salad on Dark Wh…
- Reason
- Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 23, 2019
- 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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