FDA Recall
TerminatedTerminated: January 24, 2020Historical recordClass II
Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL bag ,Rx Only , Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-237-01
by PharMEDium Services, LLC
- Reason
- Subpotent Drug
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 24, 2018Historical recordClass I
MAN OF STEEL capsules, 3000mgs/grain, 1-count packets, Packaged for: One Drop Solutions, LLC, POB 231693, Sacramento, California 95823; vitility@yahoo.com; www.manofsteelpills.com; UPC 1 0001001378 7.
by Vitility
- Reason
- Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: October 30, 2018Historical recordClass I
PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.
by Lucky Mart Inc.
- Reason
- Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 9, 2018Historical recordClass II
Norepinephrine Bitartrate16 mg added to 0.9% Sodium Chloride 250 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025014801
by Banner Pharmacy Services, LLC
- Reason
- Lack of Assurance of Sterility.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 9, 2018Historical recordClass II
VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025007001
by Banner Pharmacy Services, LLC
- Reason
- Lack of Assurance of Sterility.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 9, 2018Historical recordClass II
Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025001001.
by Banner Pharmacy Services, LLC
- Reason
- Lack of Assurance of Sterility.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 9, 2018Historical recordClass II
Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag, 125 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025018601
by Banner Pharmacy Services, LLC
- Reason
- Lack of Assurance of Sterility.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 23, 2020Historical recordClass I
General Mills, Inc
- Product
- Cascadian Farm Organic Cinnamon Raisin Granola, Net Wt 15.6…
- Reason
- General Mills is recalling 2 production runs of Cascadian Farm Organic Cinnamon Raisin Granola due to undeclared nut allergen, almond.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: January 4, 2018Historical recordClass I
Whole Foods Market Brand 365, Llc
- Product
- 365 Organic Raisin Bran Flakes 15 oz. packaged in plastic ba…
- Reason
- Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were packaged into 365 Organic Raisin Bran Flakes boxes.
- Published
- November 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: October 26, 2017Historical recordClass I
Weis Markets, Inc., Ice Cream Division
- Product
- Weis, Sunbury, PA; BLT Sandwich; 1 CT
- Reason
- The firm is recalling their Store Made BLT sandwich due to undeclared egg found in the mayonnaise ingredient. The firm received an illness complaint reporting that egg was not declared in the mayonnaise ingredient.
- Published
- November 1, 2017
- Distribution
- U.S.: PA,NJ,NY,MD,VA, DE
View recall →
FDA Recall
TerminatedTerminated: April 29, 2020Historical recordClass II
Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma Private Limited, Verna, Salcette Goa 403 722 INDIA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-5858-61.
by The Harvard Drug Group
- Reason
- Failed Impurities/Degradation Specifications: Out-of-specification result for an unknown impurity.
- Published
- October 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: September 13, 2018Historical recordClass II
Bisoprolol Fumarate tablets, 5 mg, 30-count bottles, Rx only, Manufactured by: UNICHEM LABORATORIES, LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa, 403 511, India, Marketed by: UNICHEM PHARMACEUTICALS, (USA), INC. Hasbrouck Heights, NJ 07604, NDC 29300-126-13.
by UNICHEM PHARMACEUTICALS USA INC
- Reason
- Failed Impurities/Degradation Specifications: Out of Specification for an unknown impurity was observed during the 18 month stability testing.
- Published
- October 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 16, 2017Historical recordClass II
Bel Brands USA
- Product
- Merkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 7…
- Reason
- Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being notified by customers that white plastic pieces were found in the product.
- Published
- October 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: August 16, 2018Historical recordClass II
Death Wish Coffee Company, LLC
- Product
- Death Wish Nitro Canned Cold Brew Coffee 11 oz UPC: 8515520…
- Reason
- Potential for Clostridium Botulinum
- Published
- October 25, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: December 5, 2017Historical recordClass I
La Terra Fina, Inc.
- Product
- La Terra Fina Spinach Artichoke & Parmesan Dip & Spread…
- Reason
- Undeclared allergen; egg.
- Published
- October 25, 2017
- Distribution
- U.S. distribution to the following: CA,…
View recall →
FDA Recall
TerminatedTerminated: March 15, 2019Historical recordClass III
Famotidine tablets, 10 mg, packaged in 30-count bottle, OTC, labeled as a) CVS Pharmacy Acid Controller, NDC 55111-118-30, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, Made in India, b) Equate Famotidine, NDC 49035-118-30, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716, Made in India
by Dr. Reddy's Laboratories, Inc.
- Reason
- Failed impurities/degradation specifications: Famotodine has an out of specification result for an individual related substance observed during routine stability testing of a batch for related substances -impurity 8 at 24 month stability interval.
- Published
- October 18, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: March 29, 2018Historical recordClass II
Glutamine, Arginine and Carnitine, 10/100/200mg/mL, 30 mL (Multi Dose Vial), Rx Only, For Injection, United Pharmacy Compounded, 13951 N. Haverhill Rd Ste. 120-121 West Palm Beach, FL 33417
by United Pharmacy
- Reason
- CGMP Deviations; FDA analysis deterrmined that the product does not contain glutamine and two unknown impurities were observed
- Published
- October 18, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 2, 2021Historical recordClass II
Taylor Farms New Jersey, Inc.
- Product
- Wawa Fruit & Cheese, 6oz. (170g), 1 each, rigid plastic, cla…
- Reason
- The firm was notified that an ingredient used to manufacture the recalled product may contain wood slivers.
- Published
- October 18, 2017
- Distribution
- Product is distributed to Pennsylvania,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: May 30, 2019Historical recordClass II
Pinnacle Food Group, Llc
- Product
- Birds Eye Baby Sweet Peas, Net Wt. 13 oz. (369g ), Keep Froz…
- Reason
- Product has the potential to be contaminated with Listeria monocytogenes.
- Published
- October 18, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: June 27, 2019Historical recordClass I
Silver Spring Foods, Inc.
- Product
- waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 2113…
- Reason
- Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.
- Published
- October 18, 2017
- 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.
Read the full medical disclaimer.
