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Peter Piper Pizza
Updated: May 6, 2021 12:00 PM
Covid-19 OSHA Complaint, Peter Piper Pizza, 4112 East 22nd Street, TUCSON, AZ, 85711, USA
Peter Piper Pizza, 4112 East 22nd Street, TUCSON, AZ, 85711, USA
May 6, 2021 12:00 PM
“The employer is allowing an employee who tested positive for COVID-19 to work with non-infected employees. The employer does not have a quarantine policy in place to prevent the spread of COVID-19.
Alleged Hazards: 2, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-12-21 See Less”
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Dream Bone made with peanut butter, Nashville, Arkansas, USA
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June 11, 2021 10:00 PM
“Company name: Purina Animal Nutrition
Brand name: Purina
Product recalled: Beef Cattle Feed RangeLand® 30-13 TUB
Reason of the recall: Tubs that are too soft, allowing over-consumption which can lead to urea toxicity.
FDA Recall date: June 11, 2021
Recall details: Purina Animal Nutrition is ini... See Moretiating a very limited voluntary recall of one lot of Purina® RangeLand® 30-13 (125#) beef cattle feed. This recall is being initiated as a precaution related to tubs that are too soft, allowing over-consumption, which could result in urea toxicity.
Purina Animal Nutrition received reports from customers claiming the feed may have resulted in poor health and/or death. Elevated urea levels can cause health issues and potential death in cattle. Symptoms of excess urea may include muscle tremors (especially of the face and ears), abdominal pain, frothy salivation, polyuria, and bruxism (grinding of teeth). The affected product and lot number is:
- Formula No: L3B3. Item No: 1800049-627. Description: Purina® RangeLand® 30-13 (125#). Lot Number: 1MAR19CLF1
The affected feed was manufactured by Purina Animal Nutrition on March 19, 2021. The affected Purina® feed was sold in the following states: Arizona, Arkansas, Hawaii, Idaho, Louisiana, Mississippi, New Mexico, Oklahoma, Oregon, Texas, Washington.
Customers can find the lot number on the side of each tub. Customers who purchased this product are instructed to stop feeding and to destroy or return it to the point of purchase.
Check the full recall details on fda.gov
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Tahlequah, OK, USA
June 6, 2021 3:48 PM
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Amphitrite Technology Limited - I also bought one of your battery powered Skil saws on 04/17/2021., Del City, OK, USA
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June 11, 2021 9:02 PM
“Company name: Viona Pharmaceuticals Inc.
Brand name: Viona Pharmaceuticals Inc.
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Reason of the recall: Contains Nitrosodimethylamine (NDMA) impurities
FDA Recall date: June 11, 2021
Recall details: Viona Pharmaceuticals Inc., is... See Morevoluntarily recalling 2 (two) lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg to the retail level. The 2 (two) lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg have been found to contain levels of Nitrosodimethylamine (NDMA) impurities above acceptable daily limits. This product was manufactured by Cadila Healthcare Limited, Ahmedabad, India in November 2019, for U.S. distribution by Viona Pharmaceuticals Inc.
Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables. Patients who have received impacted lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg are advised to continue taking their medication and contact their physician for advice regarding an alternative treatment.
According to the FDA, it could be dangerous for patients with this serious condition to stop taking their Metformin without first talking to their healthcare professionals. Please visit the agency’s website for more information at fda.gov To date, neither Viona Pharmaceuticals Inc., nor Cadila Healthcare Limited have received any reports of adverse events related to this recall.
The product is used as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in HDPE bottles of 100 tablets, under NDC 72578-036-01. The affected Metformin Hydrochloride Extended-Release Tablets, USP 750 mg are listed in the below table. The product can be identified as white to off-white, capsule shaped, uncoated tablets, debossed with "Z", "C" on one side and "20" on the other side. Metformin Hydrochloride Extended-Release Tablets, USP 750 mg was distributed Nationwide to Distributors.
- Metformin Hydrochloride Extended-Release Tablets, USP 750 mg. NDC No: 72578-036-01. Batch No: M915601. Exp. Date: Oct-2021.
Check the full recall details on fda.gov
Source: FDA See Less”
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This place is a fraud!, Concho, Arizona, USA
Concho, Arizona, USA
June 16, 2021 2:25 PM
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1 person found this review helpful
June 6, 2021 4:58 PM
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