FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Montana Flour & Grains, Inc
- Product
- 100% Organic Spelt Grain, packaged in 10 lbs., 25 lbs. and…
- Reason
- Organic Spelt Grain is recalled because label does not declare wheat.
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Wild Northwest Razor Clams - Custom Packed-NW Wild Products,…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Wild Steelhead Salmon - Custom Packed-NW Wild Products, 6.5…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Wild Steelhead Salmon - Custom Smoked-NW Wild Products, 6.5…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Oregon Sardines - Mustard-NW Wild Products, 6.5 oz. metal ca…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Pacific White Albacore Tuna - Custom Packed -NW Wild Product…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Wild Northwest Razor Clams - Custom Smoked-NW Wild Products,…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Pacific Black Cod- Custom Smoked -NW Wild Products, 6.5 oz.…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Northwest Wild Products
- Product
- Columbia River Chinook Salmon -Custom Packed, NW Wild Produc…
- Reason
- All canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and Razor clams with any codes starting with OC because it has the potential to be contaminated with Clostridium botulinum.
- Published
- August 31, 2016
- Distribution
- distributed in Oregon and sold to consum…
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06), b) 90-count bottles (NDC 68382-035-16), and c) 1000-count bottles, (NDC 68382-035-10), Rx only, Manufactured by : Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534.
by Zydus Pharmaceuticals USA Inc
- Reason
- Failed Dissolution Specifications: out of specification dissolution results in retained samples
- Published
- August 24, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine HCL ER Capsule USP, 150mg, packaged in a) 30-count bottles (NDC 68382-036-06), b) 90-count bottles (NDC 68382-036-16), and c) 1000-count bottles, (NDC 68382-036-10), Rx only, Manufactured by : Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534.
by Zydus Pharmaceuticals USA Inc
- Reason
- Failed Dissolution Specifications: out of specification dissolution results in retained samples
- Published
- August 24, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90
by Golden State Medical Supply Inc.
- Reason
- Failed Dissolution Specifications: Out-of-specification results in retained sample.
- Published
- August 24, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.
by Golden State Medical Supply Inc.
- Reason
- Failed Dissolution Specifications: Out-of-specification results in retained sample.
- Published
- August 24, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Glipizide 2.5 mg Extended-release tablets, 30-count bottle, Rx Only, Manufactured By: Patheon Pharmaceuticals Inc Cincinnati, OH 45237, NDC 00591-0900-30
by Actavis Inc
- Reason
- Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded dissolution specification rates for the 10 hour testing point.
- Published
- August 24, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Oregon Potato Company
- Product
- IQF 3/8" Un-Blanched Yellow Onion Dice, Frozen, item number…
- Reason
- IQF 3/8" Un-Blanched, Frozen, Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 24, 2016
- Distribution
- AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Oregon Potato Company
- Product
- IQF 3/4" Yellow Onion Dice, Frozen, item number 101430, bulk…
- Reason
- IQF 3/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 24, 2016
- Distribution
- AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Oregon Potato Company
- Product
- IQF 3/8" Yellow Onion Strip, Frozen, Item number 103331, bul…
- Reason
- IQF 3/8" Frozen Yellow Onion Strip and IQF 3/8" Yellow ORGANIC Onion Strip are voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 24, 2016
- Distribution
- AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Oregon Potato Company
- Product
- 3/8" White Onion Dice- FRESH, item number 105197, bulk tote,…
- Reason
- 3/8" White Onion Dice- FRESH is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 24, 2016
- Distribution
- AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Oregon Potato Company
- Product
- IQF 1/4" Yellow Onion Dice, frozen, item numbers: 103364, 10…
- Reason
- IQF 1/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 24, 2016
- Distribution
- AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Oregon Potato Company
- Product
- 705000 IQF 3/8" Dice Yellow Onion, item number 101472, bulk…
- Reason
- 3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 24, 2016
- Distribution
- AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…
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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