FDA Recall
🇺🇸 United States
TerminatedTerminated: March 27, 2017Historical recordClass II
Cumberland Valley Creamery, LLC
- Product
- Dutchland Homestead Farmer's Cheese, Net Weight 8 oz., Handc…
- Reason
- Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
- Published
- April 5, 2017
- Distribution
- MD and PA
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 27, 2017Historical recordClass II
Cumberland Valley Creamery, LLC
- Product
- Dutchland Homestead Mozzarella, Net Weight 8 oz., Handcrafte…
- Reason
- Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
- Published
- April 5, 2017
- Distribution
- MD and PA
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: March 27, 2017Historical recordClass II
Cumberland Valley Creamery, LLC
- Product
- Luqman Cheese, White Colby, Net Wt. 8 oz.., Distributed by:…
- Reason
- Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
- Published
- April 5, 2017
- Distribution
- MD and PA
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: March 27, 2017Historical recordClass II
Cumberland Valley Creamery, LLC
- Product
- Luqman Cheese, White Cheddar, Net Wt. 8 oz.., Distributed by…
- Reason
- Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
- Published
- April 5, 2017
- Distribution
- MD and PA
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: March 27, 2017Historical recordClass II
Cumberland Valley Creamery, LLC
- Product
- Luqman Cheese, Monterey Jack, Net Wt. 8 oz.., Distributed by…
- Reason
- Multiple laboratory analysis found multiple instances where various cheeses exceed allowed limits of generic E. coli.
- Published
- April 5, 2017
- Distribution
- MD and PA
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: March 27, 2017Historical recordClass I
Seafood Avenue
- Product
- DH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH.…
- Reason
- Product may have the potential for pathogen growth and toxin formation due to Clostridium botulinum.
- Published
- April 5, 2017
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: April 20, 2017Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- The Bakery Mini Pecan Tarts Part Platter NET WT 16x 16.2 OZ…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 20, 2017Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item num…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 20, 2017Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) it…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: April 20, 2017Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- Two-Bite Pecan Tart 9.2 oz (261g) item number 02023; NL Two-…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 14, 2017Historical recordClass II
Pinnacle Foods
- Product
- Buffalo Blue Kettle Cooked Potato Chips 8 oz (227g)
- Reason
- Snyder of Berlin is recalling their Buffalo Blue Kettle Cooked Potato Chips after being informed that a milk powder used within a spice blend ingredient may contain Salmonella.
- Published
- April 5, 2017
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: March 1, 2019Historical recordClass I
Life Rising Corp S
- Product
- The product is packaged in a white plastic bottle with green…
- Reason
- The dietary supplement contains lead.
- Published
- April 5, 2017
- Distribution
- This product was shipped to IL, OK, FL,…
View recall →
FDA Recall
TerminatedTerminated: July 2, 2018Historical recordClass II
Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60
by Fougera Pharmaceuticals Inc.
- Reason
- Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
- Published
- March 29, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 23, 2018Historical recordClass II
Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC 62756-015-40
by Sun Pharmaceutical Industries, Inc.
- Reason
- Presence of Particulate Matter
- Published
- March 29, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: June 1, 2022Historical recordClass II
Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13
by AVKARE Inc.
- Reason
- Failed impurities/ degradation specifications: Product was above specification for unknown impurities.
- Published
- March 29, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: May 31, 2019Historical recordClass III
Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-30).
by PFIZER INC
- Reason
- Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
- Published
- March 29, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 31, 2019Historical recordClass III
Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-205-25).
by PFIZER INC
- Reason
- Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
- Published
- March 29, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: May 31, 2019Historical recordClass III
Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-10).
by PFIZER INC
- Reason
- Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
- Published
- March 29, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 23, 2019Historical recordClass II
ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.
by Legacy Pharmaceutical Packaging LLC
- Reason
- Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
- Published
- March 29, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: November 5, 2019Historical recordClass II
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.
by Zydus Pharmaceuticals USA Inc
- Reason
- Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
- Published
- March 29, 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.
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