FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
SM Fish Corp.
- Product
- OSSIE'S STIGLITZ HERRING, NET WT. 7 OZ., UPC 739885109064; -…
- Reason
- The products have the potential to be contaminated with Listeria monocytogenes based on the findings of the bacteria in the plant via FDA environmental sampling plus the district's inspectional findings
- Published
- November 2, 2016
- Distribution
- New York and New Jersey via retail store…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
SM Fish Corp.
- Product
- OSSIE'S TAAM SHABBOS HERRING, NET WT. 7 OZ., UPC 73988510905…
- Reason
- The products have the potential to be contaminated with Listeria monocytogenes based on the findings of the bacteria in the plant via FDA environmental sampling plus the district's inspectional findings
- Published
- November 2, 2016
- Distribution
- New York and New Jersey via retail store…
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FDA Recall
Terminated
Historical recordClass II
Trokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850, NDC 17772-102-15
by Supernus Pharmaceuticals, Inc.
- Reason
- Superpotent Drug: Failure of assay specifications in the capsule.
- Published
- October 26, 2016
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
PARICALCITOL Capsules, 4 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7658-56.
by Teva Pharmaceuticals USA
- Reason
- Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.
- Published
- October 26, 2016
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
PARICALCITOL Capsules, 2 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7657-56.
by Teva Pharmaceuticals USA
- Reason
- Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.
- Published
- October 26, 2016
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
PARICALCITOL Capsules, 1 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7656-56.
by Teva Pharmaceuticals USA
- Reason
- Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.
- Published
- October 26, 2016
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass I
Super Samurai-X , 1000 mg, 1 capsule per pack , 24 single packs per box.
by SOS Telecom Inc.
- Reason
- Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
- Published
- October 26, 2016
- Distribution
- NY
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FDA Recall
Terminated
Historical recordClass I
Ginseng Power-X , 1800 mg, 1 capsule per pack , 24 single packs per box.
by SOS Telecom Inc.
- Reason
- Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
- Published
- October 26, 2016
- Distribution
- NY
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FDA Recall
Terminated
Historical recordClass I
Ninja-X, 4200 mg, 1 capsule per pack, 24 single packs per box.
by SOS Telecom Inc.
- Reason
- Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
- Published
- October 26, 2016
- Distribution
- NY
View recall →
FDA Recall
Terminated
Historical recordClass I
Tiger-X, 1200 mg, 1 capsule per pack , 24 single packs per box
by SOS Telecom Inc.
- Reason
- Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements
- Published
- October 26, 2016
- Distribution
- NY
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
National Foods Packaging Inc
- Product
- National Foods Packaging Low Sodium Chicken Base in 50 lb wh…
- Reason
- Product contains a spice which was tested and found to contain elevated levels of lead.
- Published
- October 26, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
National Foods Packaging Inc
- Product
- National Foods Packaging Chicken Base in 25 lb white poly-li…
- Reason
- Product contains a spice which was tested and found to contain elevated levels of lead.
- Published
- October 26, 2016
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
National Foods Packaging Inc
- Product
- Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined b…
- Reason
- Product contains a spice which was tested and found to contain elevated levels of lead.
- Published
- October 26, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd.
- Product
- ATLANTIC Smoked SALMON Whole, Net Wt. 8 OZ (225.89), Keep Re…
- Reason
- Environmental samples collected by the Food and Drug Administration revealed the presence of Listeria monocytogenes which has the potential to contaminate food products.
- Published
- October 26, 2016
- Distribution
- CT & NY via retail stores
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd.
- Product
- Sliced - Smoked ATLANTIC SALMON, Net Wt. 8 OZ (225.89), Keep…
- Reason
- Environmental samples collected by the Food and Drug Administration revealed the presence of Listeria monocytogenes which has the potential to contaminate food products.
- Published
- October 26, 2016
- Distribution
- CT & NY via retail stores
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
DNE Nutraceuticals Inc.
- Product
- Adwe Naturals Prenatal Vitamin Manufactured for: Adwe Labora…
- Reason
- Adwe Prenatal tablets are being recalled due to a concern of potency of folic acid.
- Published
- October 26, 2016
- Distribution
- NY
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Food Gusto, Inc.
- Product
- Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed pla…
- Reason
- Birdy 3 in 1 Coffee Mix (Robusta) may contain undeclared milk allergen and the nutritional labeling is unclear.
- Published
- October 26, 2016
- Distribution
- CT, MA and NY
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Dollar General Corporation
- Product
- Cookies Bergen, Soft Baked Chocolate Brownie Cookies, NET WE…
- Reason
- Mold found in cookie product
- Published
- October 26, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Natures One Inc
- Product
- Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nut…
- Reason
- The firm received complaints that the wrong size scoop was in the product canister. Use of this scoop would only yield 60% nutrition instead of 100% nutrition.
- Published
- October 26, 2016
- Distribution
- Product was shipped to the following sta…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
BIMBO Bakeries USA Inc.
- Product
- Entenmann's Little Bites Fudge Brownies - 20 muffins, 5 Pouc…
- Reason
- Presence of plastic in muffins and brownies.
- Published
- October 26, 2016
- 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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