FDA Recall
Terminated
Historical recordClass II
All sterile drug preparations remaining within expiry prepared from Morphine Sulfate PF Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
by Intrathecal Compounding Specialist, LLC
- Reason
- Lack of sterility assurance.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between October 16, 2017 and November 17, 2017, Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
by Intrathecal Compounding Specialist, LLC
- Reason
- Lack of sterility assurance.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
All sterile drug preparations remaining within expiry prepared from Fentanyl Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017 Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.
by Intrathecal Compounding Specialist, LLC
- Reason
- Lack of sterility assurance.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 g tubes (NDC 0713-0638-31); and c) 90 g tubes (NDC 0713-0638-18), Rx Only, Manufactured by: G&W Laboratories, Inc., South Plainfield, NJ 07080.
by G & W Laboratories, Inc.
- Reason
- Discoloration: Product is supposed to be a white to off white homogenous cream and may have intermittent yellow discoloration.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Panera, LLC
- Product
- Reduced-Fat Wild Blueberry Cream Cheese, 2 oz. and 8 oz.
- Reason
- Product may be contaminated with Listeria monocytogenes.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Panera, LLC
- Product
- Panera Reduced-Fat Honey Walnut Cream Cheese, 2 oz. and 8 oz…
- Reason
- Product may be contaminated with Listeria monocytogenes.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Panera, LLC
- Product
- Panera Chive&Onion Reduced Fat Cream Cheese Spread, 2 oz. an…
- Reason
- Product may be contaminated with Listeria monocytogenes.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Ventura Foods Llc
- Product
- SunGlow, European Style Butter Blend Margarine, packaged in…
- Reason
- SunGlow contains undeclared soy lecithin.
- Published
- February 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Ventura Foods Llc
- Product
- SunGlow, Unsalted European Style Butter Blend Margarine (169…
- Reason
- SunGlow contains undeclared soy lecithin.
- Published
- February 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Mountain Rose Inc
- Product
- Prickly Ash Bark Powder Herbal Supplement, packaged in food…
- Reason
- Prickly Ash Bark Powder is recalled due to a potential contamination with Salmonella.
- Published
- February 14, 2018
- Distribution
- distributed in AK, AR, AZ, CA, CO , FL,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Simply Delicious, Inc. dba Bobo's Oat Bars
- Product
- Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per…
- Reason
- Bobo's recalled Coconut 3oz Bar due to mold.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Panera, LLC
- Product
- Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
- Reason
- Product may be contaminated with Listeria monocytogenes.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Panera, LLC
- Product
- Panera Plain Cream Cheese, 2 oz. and 8 oz.
- Reason
- Product may be contaminated with Listeria monocytogenes.
- Published
- February 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Bulletproof 360 Inc
- Product
- Bulletproof Unflavored Collagen Protein High Performance Bui…
- Reason
- Bulletproof Collagen Protein is recalled due to undeclared milk. The actual product inside the package is whey (milk) protein but mis-labeled as collagen protein.
- Published
- February 14, 2018
- Distribution
- distributed in CA, CO, CT, FL, GA, IA, I…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
CHOBANI
- Product
- Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogur…
- Reason
- Product is recalled because a statement on the overwrap label erroneously states "No Gluten" while the ingredients statement and the Contains statements on both the overwrap label and the flip label on each individual cup declare wheat.
- Published
- February 14, 2018
- Distribution
- distributed in AL, AR, AZ, CA, CO, CT,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Palmer and Company
- Product
- Sea Salt Caramel Hearts, Net Wt 12 OZ (340 g), Made by Palme…
- Reason
- During packaging, the firm observed a peanut stuck to the outside of caramel heart. Peanuts are not declared on the label.
- Published
- February 14, 2018
- Distribution
- Product distributed to one distribution…
View recall →
FDA Recall
Terminated
Historical recordClass I
Nexterone (amiodarone HCl) Premixed Injection, 150mg/100mL, 100-mL bag, Rx Only, Sterile, Baxter Healthcare Corporation, Deerfield, IL. NDC 43066-150-10
by Baxter Healthcare Corporation
- Reason
- Presence of Particulate Matter:Particulate identified as polyethylene, the primary constituent of the film and ports used to manufacture the bag in which product is packaged
- Published
- February 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass I
Clopidogrel Tablets, USP 75 mg, 30-count bottles, Rx only, Packaged for: International Laboratories, LLC St. Petersburg, FL 33710, NDC 54458-888-16
by International Laboratories, LLC
- Reason
- LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles labeled as Clopidogrel tablets, USP 75 mg.
- Published
- February 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Vecuronium bromide for Injection, 10 mg vials, Rx only, Mfd. for: Fresenius Kabi, Lake Zurich, IL 60047, Made in India, NDC 63323-781-10
by Fresenius Kabi USA, LLC
- Reason
- Failed impurities/ degradation specifications: Out-of-specification (OOS) result for USP related compound F at the 12 month stability test station.
- Published
- February 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Atorvastatin Calcium Tablets 40 mg, 90 count bottles, Rx only, Mfd by: Dr. Reddy's Laboratories, Ltd., Srikakulam, INDIA --- NDC 55111-123-05
by Dr. Reddy's Laboratories, Inc.
- Reason
- Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability
- Published
- February 7, 2018
- 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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