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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Petmatrix Dreambone Dino Chews, Yulee, FL, USA

April 27, 2021 9:13 AM

Yulee, Florida, United States

Symptoms: Vomiting Other

We gave our dog the Dreambone Dino Chews on Sunday. On Tuesday we noticed he was wanting to go into his kennel and sleep. Tuesday evening he was acting odd with jerking movement, sticking his tongue out, oddly staring at the ceiling and refusing to drink water. We immediately took him to the vet where they induced vomiting, gave him antibiotics and an IV. He continued to not drink water in his own and show neurological behaviors that our vet said was focal seizures, lip-licking and star-gazing. The Dreambone treats were the only change in his diet. He would not drink water on his own for at least 3 days and he had focal seizures on and off for about 5 days. Do not give your dog any Petmatrix, Spectrum, or Dreambone product. They will poison your beloved pet. They package says they are made in China and when you google the company they are also made in Vietnam.

Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Doctor visit
More incidents from:
Yulee
Florida
United States

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Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

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The NDC, Lot Number, Expiration Date, and Configuration details for Sterile Water for Injection, USP, is indicated in the table below and a photo of the product can be found at the end of this press release. The product lot was distributed nationwide to wholesalers/distributors/and hospitals in the United States from October to December 2020.

- Sterile Water for Injection, USP 100 mLbr Single-dose Glass Fliptop Vial. NDC: Vial: 0409-4887-25 | Carton: 0409-4887-99. Lot Number: DN9185. Expiration Date. 01 Apr 2023. Presentation: 100 mL, Single-dose Glass Fliptop Vial. Configuration: Tray of 25 vials.

Hospira, Inc., places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Hospira, Inc. has notified wholesalers/ distributors/hospitals by letter to arrange for return of any recalled product.

Wholesalers, distributors or hospitals with an existing inventory of the lot, which is being recalled, should stop use and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or hospital level/institution, please notify any accounts or additional locations which may have received the recalled product from you. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall. For additional assistance, call Stericycle at 1-800-805-3093 between the hours of 8 a.m. to 5 p.m. ET, Monday through Friday.

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Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User