FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Pinnacle Food Group, Llc
- Product
- Wish Bone House Italian Salad Dressing 15 oz.
- Reason
- The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.
- Published
- July 18, 2018
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Nectar Foods LLC
- Product
- Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in q…
- Reason
- Honey Mama's Oregon Peppermint Cacao-Nectar Bar, 2.5 oz, is recalled due to undeclared almonds.
- Published
- July 18, 2018
- Distribution
- Product is sold on website HoneyMamas.co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Earthrise Nutritionals Llc
- Product
- Earthrise Natural Spirulina; Net Weight: 20.0 kg( 44.0 lbs);…
- Reason
- The product may contain small metal pieces (approximately 2 mm to 8 mm) from a sifter screen.
- Published
- July 18, 2018
- Distribution
- CA, AZ, UT, HI, OR. WA, MO, NY, TX, IL,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Brew Dr Kombucha, LLC
- Product
- Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bo…
- Reason
- Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
- Published
- July 18, 2018
- Distribution
- distributed in CA, CO, NY, OR, WA, and W…
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FDA Recall
Terminated
Historical recordClass I
Neostigmine Methylsulfate Injection Solution, 3 mg per 3 mL, 1 mg per mL, 3 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-01.
by Fagron Compounding Services LLC dba Fagron Sterile Services
- Reason
- Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3 mL.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass I
Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-02.
by Fagron Compounding Services LLC dba Fagron Sterile Services
- Reason
- Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3 mL.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic Laxative, OTC, packaged in a) 119 g bottle (NDC 49035-312-07), b) 238 g bottle (NDC 49035-312-08), Distributed by: Wal-mart Stores, Inc., Bentonville, AR 72716
by LUPIN SOMERSET
- Reason
- Labeling: Not Elsewhere Classified - A private label distributor noted unfiled NDC numbers on EQ ClearLax Polyethylene Glycol 3350 NF Powder Solution of various sizes.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01
by Qualgen, LLC
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass III
ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01
by Qualgen, LLC
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass II
Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-401-02.
by Ingenus Pharmaceuticals Llc
- Reason
- Superpotent Drug: High out of specification assay value results for potency.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass II
Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-402-05.
by Ingenus Pharmaceuticals Llc
- Reason
- Superpotent Drug: High out of specification assay value results for potency.
- Published
- July 11, 2018
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Icelandic Provisions Inc.
- Product
- Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC:…
- Reason
- Cups containing coconut skyr yogurt may have been mislabeled as vanilla skyr yogurt.
- Published
- July 11, 2018
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Four Link Nutriworld
- Product
- BLUEBERRY PRETZEL, NET WEIGHT : 4OZ (113g) ,USE BY DATE : 12…
- Reason
- Four Link Nutriworld has initiated a recall of NATURAL WHOLE NUT - BLUEBERRY PRETZEL, 4.0z, used by date of 12/01/2018 because of mislabeled product. The "MILK" ingredient was omitted in the ingredient section. Blueberry Pretzel has a coating that includes milk content. This can cause milk allergen to people who are allergic to milk.
- Published
- July 4, 2018
- Distribution
- The product was distributed to only NY a…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Utz Quality Food Inc
- Product
- Good Health Organic Tortillas; Black Bean & Rice; Net Wt 5.5…
- Reason
- Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
- Published
- July 4, 2018
- Distribution
- AL AL AR AZ CT DC DE FL GA IL…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Utz Quality Food Inc
- Product
- Golden Flake TORTIYAHS! Superior Dipping Chips; Net Wt 12.5…
- Reason
- Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
- Published
- July 4, 2018
- Distribution
- AL AL AR AZ CT DC DE FL GA IL…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Utz Quality Food Inc
- Product
- Weis Signature Collection No Salt Added White Corn Tortilla…
- Reason
- Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
- Published
- July 4, 2018
- Distribution
- AL AL AR AZ CT DC DE FL GA IL…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Utz Quality Food Inc
- Product
- Utz Organic Yellow Corn Tortillas, Net Wt 9 oz; UTZ Quality…
- Reason
- Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
- Published
- July 4, 2018
- Distribution
- AL AL AR AZ CT DC DE FL GA IL…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Utz Quality Food Inc
- Product
- Utz Organic Blue Corn Tortillas; Net Wt 9 oz; UTZ Quality Fo…
- Reason
- Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen.
- Published
- July 4, 2018
- Distribution
- AL AL AR AZ CT DC DE FL GA IL…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Golden Star Wholesale Inc
- Product
- Al Reef dried apricot sour, 12 oz., packed in plastic, 24 pa…
- Reason
- Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried apricot sour, 12 oz., due to undeclared sulfites.
- Published
- July 4, 2018
- Distribution
- Domestic: MI, NY,MN,KY,WI,FL,NC,VA,OR,MA…
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FDA Recall
🇺🇸 United States
Ongoing
Historical recordClass III
Absonutrix
- Product
- Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bott…
- Reason
- The firm was informed that the product did not contain vitamin B12 (Methylcobalamyn) as listed on the label.
- Published
- July 4, 2018
- Distribution
- Product was shipped to the following sta…
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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