FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Chipotle Cheese Packaged in the fol…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Cheese Packaged in the following si…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Habanero Cheese Packaged in the fol…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Morel & Leek Cheese Packaged in the…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Onion & Chives Cheese Net Wt. 1 lb.
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Ghost Pepper Cheese packaged in the…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Pueblo Cheese packaged in the follo…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Jalapeno Cheese packaged in the fol…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Tomato Basil Cheese, Net Wt. 40 lb…
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 19, 2019Historical recordClass III
Springside Cheese Corp
- Product
- Springside Monterey Jack Garden Vegetable Cheese, 40 lbs.
- Reason
- Various cheeses are being recalled because they may have been made with milk that was held for 13.8 seconds during pasteurization.
- Published
- March 14, 2018
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: November 14, 2018Historical recordClass I
Lotte International America Corp.
- Product
- Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g…
- Reason
- Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
OngoingHistorical recordClass II
Snyder's-Lance Inc.
- Product
- Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable po…
- Reason
- Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans.
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 24, 2018Historical recordClass II
Vitalab Co Inc
- Product
- Product packaged in the following ways A) Sonne's, No. 17, N…
- Reason
- The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
- Published
- March 14, 2018
- Distribution
- Product distributed to consumers, distri…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: July 30, 2018Historical recordClass II
Get The Tea
- Product
- Life Change Fat Burner, 90 Gel Caps!, Burn Fat!, Remove fat…
- Reason
- Get The Tea is notifying customers that Life Change Fat Burners contain soy.
- Published
- March 14, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 1, 2020Historical recordClass I
Levofloxacin in 5% Dextrose Injection, 250 mg/50 mL (5 mg/mL), 50 mL Single-Use flexible container, Rx Only, Manufactured for: AuroMedics Pharma LLC 6 Wheeling Drive, Dayton, NJ 08810 Manufactured for: Aurobindo Pharma Limited IDA, Pashamylaram - 502307, India ---- NDC 55150-243-46
by AuroMedics Pharma LLC
- Reason
- Presence of Particulate Matter; contains visible particulate matter identified as mold.
- Published
- March 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: August 7, 2019Historical recordClass I
GERICARE Eyewash, sterile eye irrigating solution, packaged in a 4 fl oz (118 mL) bottle, OTC, Distributed by Geri-Care Pharmaceuticals Corp., Brooklyn, NY 11204, NDC 57896-0186-04
by Kareway Products Inc
- Reason
- Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans
- Published
- March 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: January 23, 2020Historical recordClass II
0.9% Sodium Chloride Irrigation USP, 1000 mL Plastic Irrigation Container (PIC), Rx only, B. Braun Medical Inc., Irvine, CA 92614, Catalog # R5200-01, NDC 0264-2201-00.
by B. Braun Medical Inc
- Reason
- Presence of Particulate Matter: Customer complaint of particulate matter which has been identified as polyethylene, which is consistent with the material used to manufacture the container cap was received.
- Published
- March 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: September 10, 2019Historical recordClass II
SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by Fagron Inc. St. Paul, MN 55120
by Fagron, Inc
- Reason
- Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).
- Published
- March 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 29, 2020Historical recordClass II
PVP Scrub Solution, Povidone Iodine, 7.5% (equivalent to 0.75% available iodine), 4 FL OZ bottle, Manufactured in USA by Medline Industries, Inc., Northfield, IL 60093; Product Number MDS093945; NDC 53329-938-04
by Medline Industries Inc
- Reason
- Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.
- Published
- March 7, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 8, 2020Historical recordClass II
INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL), Rx Only, packaged in a) single dose vials, (NDC 52544-931-07), b) carton of 10 x 2 ml Single Dose Vials (NDC 52544-931-02) Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054, Manufactured by: Patheon Italia S.p.A. Ferentino, Italy 03013.
by ALLERGAN
- Reason
- Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
- Published
- March 7, 2018
- 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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