FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- The Ultimate Wine and Champagne Collection Basket #399
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Cakebread Cellars Napa Valley Duet Basket #396
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- California Cabernet and Chardonnay Gift Basket #361
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Bodega de San Antonio Sangria Traditional Basket #298
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Napa & Sonoma Valley Exclusive Basket #141
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Wine Trio Basket #050
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Metal Basket with Leather Handles SKU #54506-6
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- The Executive with Houdini Blue Cheese Twists, 7 ounces COM…
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Metal Basket with Handles with Houdini Blue Cheese Twists, 7…
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Woven Lacquer Treat Basket with Blue Cheese Savory twist ite…
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Sweets For The Season gift basket, Item No. 1081594
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Tis The Season gift basket, Item No. 1084804
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Wooden Centerpiece gift basket, Item No. 1080571
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Houdini Fabric gift basket, Item No. 1072552
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Houdini Inc.
- Product
- Vintners Path Chardonnay Seasons Greetings Basket #795
- Reason
- Potential Salmonella contamination.
- Published
- February 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Azelastine Hydrochloride Nasal Solution (Nasal Spray), 0.1% (137 mcg per spray), packaged in 30 mL bottles, Rx only, Distributed by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-0293-99
by Roxane Laboratories, Inc.
- Reason
- Defective Delivery System: out of specification result for droplet size distribution at the d90 measurement testing during the 6 month time point..
- Published
- February 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
buPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, 60 count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India NDC 47335-0738-86
by Sun Pharmaceutical Industries, Inc.
- Reason
- Failed Dissolution Specifications; 18 month stability time point
- Published
- February 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
buPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, a) 60 (NDC 47335-737-86), b) 100 (NDC 47335-737-88) and c) 500 (NDC 47335-737-13) count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India
by Sun Pharmaceutical Industries, Inc.
- Reason
- Failed Dissolution Specifications; 18 month stability time point
- Published
- February 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Temozolomide Capsules, 250 mg, 5-count bottles, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA, NDC 0378-5265-98.
by Mylan LLC.
- Reason
- Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
- Published
- February 1, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Temozolomide Capsules, 180 mg, packaged in a) 5-count bottles (NDC 0378-5264-98), b) 14-count bottles (NDC 0378-5264-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
by Mylan LLC.
- Reason
- Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
- Published
- February 1, 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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