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The CDC announced that they are currently investigating a multistate outbreak of Salmonella Uganda infections linked to Pet Bearded Dragons. As of January 10, 2022, 44 people infected with the outbreak strain of Salmonella Uganda have been reported from 25 states (AL, AR, CA, CT,FL, KS, LA,... See More MA, MN, MO, MT, NE, NM, NV, NY, OR, PA, RI, SC, SD, TX, UT, VA, WA, WI). 15 people of the total have required hospitalization but no deaths have been reported to date.

Illnesses started on dates ranging from December 24, 2020, to December 2, 2021. According to the outbreak notice, Bearded dragons can carry Salmonella germs in their droppings even if they look healthy and clean. These germs can easily spread to their bodies and anything in the area where they live and roam. You can get sick from touching your bearded dragon or anything in its environment and then touching your mouth and swallowing Salmonella germs.

CDC advises always take these steps to stay healthy around your pet bearded dragon:

- Always wash hands thoroughly with soap and water right after touching or feeding your bearded dragon and after touching or cleaning the area where it lives and roams.
- Don’t kiss or snuggle your bearded dragon, and don’t eat or drink around it. This can spread Salmonella germs to your mouth and make you sick.
- Keep your bearded dragon out of your kitchen and other areas where you eat, store, or prepare food.
- Clean your bearded dragon supplies outside the house, if possible. These supplies may include its feeders, toys, and food and water containers. If you clean the supplies indoors, don’t clean them in the kitchen or other areas where you eat or prepare food. Use a laundry sink or bathtub, and thoroughly clean and disinfect the area right after.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance.

Check the CDC website for the full investigation details on: cdc.gov

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Oscor Inc. is voluntarily recalling 14 lots of Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 down to the user level. The Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 have been found to have increased risk of the hub cap and seal... See More on the proximal end of the device handle detaching during use.

RISK STATEMENT: The Destino Twist 14T Model DST1405525 & Guidestar 14F Model D141103 detachment of the hub cap and seal could lead to bleeding at the proximal end of the device and/or air embolism for the patient during intracardiac, renal or other peripheral placements procedures.

Oscor Inc. has reported two (2) Medical Device Reports to the FDA related to detachment of hub cap and seal on the proximal end of the device handle. The recall is limited to the two model numbers and lot numbers outlined above. There are no other recalls associated with this product.

PRODUCT INFORMATION: The product is steerable guiding sheath intended for the introduction of diagnostic and therapeutic devices into the human vascular, including but not limited to intracardiac, renal or other peripheral placements; it cannot be use for neural placements. The product is provided sterile, one unit per pouch / tray for details and can be identified on the printed labeling with the information below (1, 2, and 3).

The affected Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 were distributed Worldwide to distributors and hospitals from June 8, 2021 to November 30, 2021.

Recalled Product Impacted (1)

- Destino Twist 14F (DST1405525). UDI Number: 885672011123. Lot Number: PQOC13475. Expiration Date 10-01-2021. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14073. Expiration Date 11-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14072. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14071. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13834. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13828. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13827. Expiration Date 08-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12995. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12632. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12633. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12345. Expiration Date 06-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12330. Expiration Date 06-01-2025. Packaging State Type: Sterile.

Destino 14F Twist Model (2)

Product: Destino Twist 14F
GTIN (Unit): 00885672011123
Model: DST1405525
Sheath & Dilator: S55CM D73CM
French Size: 14F
Quantity: 6 Units

Guidestar 14F - Model (3)

Product: Guidestar 14F
GTIN (Unit): 00885672010911
Model: D141103
Sheath & Dilator: S71CM D89CM
French Size: 14F
Quantity: 543 Units

Company name: Oscor Inc.
Brand name: Oscor
Recalled: Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 steerable guiding sheath
Reason of the recall: Hub cap and seal on the proximal end of the device handle may detach during use
FDA Recall date: January 12, 2022

Check the full recall details on fda.gov

Source: FDA See Less

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For the past year, almost all personal or holiday cards sent through USPS in Clifton, NJ have been opened and checks, money, or lottery tickets have been removed. The opened envelopes (sometimes torn) are then delivered. Whether the destination is in-state or out-of-state, if mailed in Clifton,... See More envelopes are opened or never arrive. However, if mailed in any town other than Clifton, envelopes arrive at their stated destination and are always intact. Almost all of this mail passes through the Daniels Sectional facility, but only mail sent through Clifton disappears or is vandalized. Many individuals are experiencing problems, which include stealing and modifying checks with attempts to cash them. Bills went unpaid because the checks never arrived. Dusturbingly, a check was removed from a birthday card deposited in the mailbox directly outside the Post Office at 1114 Main Avenue. See Less

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Ordered a custom blanket for my nana for Christmas. Ordered it a month ago and i got a message that it is lost in new jersey. It was last scanned on nov 20 2021. I dont have the time to re order it because Christmas is this week! Ruined my gift. See Less

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Woody’s Pet Food Deli is recalling Raw Cornish Hen pet food “With Supplements” sticker due to a Salmonella health risk. The product was distributed in the company’s retail stores in Minneapolis, Saint Paul, and Woodbury, Minnesota.

Salmonella can affect animals eating the product and there is risk... See More to humans from handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

- Woody’s Pet Food Deli RAW CORNISH HEN with SUPPLEMENTS (5 lb. plastic tub). PLU Code 5230. Expiration date 11/20/22
- Woody’s Pet Food Deli RAW CORNISH HEN with SUPPLEMENTS (15 oz. plastic container). PLU Code 1652. Expiration date 11/20/22

Two (2) 5lb tubs were sold in the company’s St Paul store. Twelve (12) 15oz containers were distributed through its 3 Twin Cities, MN retail stores.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping, and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms.

Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

The company continues their investigation as to the source of the problem and will resume production when the problem is resolved. The recall is a result of FDA sampling due to a consumer complaint on another product, which testing revealed a sample of this product contains Salmonella.

Consumers who have these products should discontinue use and may return the unused portion to the place of purchase for a full refund. If you have recalled product in your home, clean refrigerators/freezers where the product was stored and clean and disinfect all bowls, utensils, food prep surfaces, pet bedding, toys, floors, and any other surfaces that the food or pet may have had contact with. Because animals can shed the bacteria in the feces when they have bowel movements, it’s particularly important to clean up the animal’s feces in yards or parks where people or other animals may become exposed, in addition to cleaning items in the home. Consumers should thoroughly wash their hands after handling the affected product or cleaning up potentially contaminated items and surfaces.

Company name: Woody’s Pet Food Deli
Brand name: Woody's Pet Food Deli
Product recalled: Raw Cornish Hen pet food “With Supplements”
Reason of the recall: Potential Salmonella
FDA Recall date: December 23, 2021

Check the full recall details on fda.gov

Source: FDA See Less

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Lohxa LLC is voluntarily recalling one lot of Senna Syrup 8.8mg/5mL, unit-dose cups to the consumer level. The product is being recalled due to microbial contamination. Use of contaminated product by the elderly, patients with a weakened immune system, or patients at a higher risk of developing... See More life-threatening inflammation of the heart, could result in infections that could be life-threatening.

To date, Lohxa LLC has not received any reports of adverse events related to this recall.

The product is used as a natural vegetable laxative for the relief of occasional constipation and is packaged into 5 mL unit-dose cups. The product is distributed into cases of 20 cartons packaged with 24 units each, NDC: 50268-731-24. The affected Senna Syrup 8.8mg/5mL lot is AM1115S with expiration date of 01/2023. The product can be identified by the label attached.

Product was distributed to AvKare (Wholesaler) who may have further distributed this to clinics, hospitals, and healthcare providers. Outer carton labeling (see images) Unit-Dose Cups (see image) Lohxa LLC is notifying its distributors and customers by letter and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using the product and return it to place of purchase.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Lohxa LLC
Brand name: AVpak
Product recalled: Senna Syrup 5mL
Reason of the recall: Potential microbial contamination
FDA Recall date: January 12, 2022

Check the full recall details on fda.gov

Source: FDA See Less

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My tracking number has not been updated in a month. Package is nowhere to be found.
9405508205497905600301 See Less

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Package ID: 0652097001
Delivery conf at Teterboro: 92748909840515553021375525
Ordered small package that has been sitting at Teterboro since 12/8/21…it’s been a month and still not delivered. This is ridiculous!!!!! See Less

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I turned on the water and small black spots appeared as I was pouring it in a white cup. Then the water when I turned it on a little bit looked murky white. See Less

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Padagis US LLC announced today it has issued a voluntary nationwide recall to the consumer/user level of the lots of Nitroglycerin Lingual Spray listed in the table below. Out of an abundance of caution, this product is being recalled from the market due to a complaint received... See More that a unit may not dispense.

There is a risk that the product may not properly dispense medication to patients in the event of a malfunction of their dispensing unit. This recall applies only to the 12g spray bottle and not the 4.9g spray bottle of this medication.

- Drug: Nitroglycerin Lingual Spray
- NDC: 45802-210-02
- Strength: 400 mcg per spray
- Net Contents: 12g
- Lot # 150892
- Expiration: Oct 2022

- Drug: Nitroglycerin Lingual Spray
- NDC: 45802-210-02
- Strength: 400 mcg per spray
- Net Contents: 12g
- Lot # 153199
- Expiration: Feb 2023

- Drug: Nitroglycerin Lingual Spray
- NDC: 45802-210-02
- Strength: 400 mcg per spray
- Net Contents: 12g
- Lot # 156041
- Expiration: Apr 2023

Company name: Padagis
Brand name: Perrigo
Product recalled: Nitroglycerin Lingual Spray
Reason of the recall: Unit may not properly dispense medication.
FDA Recall date: December 27, 2021

If the product does not deliver the appropriate amount of nitroglycerin, the patient will likely continue to experience chest pain. The label advises that if relief is not obtained after 3 doses over 15 minutes the patient should promptly seek medical attention. To date, Padagis has not received any reports of adverse events related to this recall.

Nitroglycerin Lingual Spray is indicated for acute relief of an attack or prophylaxis of chest pain due to coronary artery disease in adult patients. All packaging and branding on affected units is that of Perrigo Company PLC. The product is packaged in a 12 g bottle contained within a carton. The medication was distributed Nationwide in the USA to wholesalers and retailers.

Healthcare providers, distributors, and retailers that have product which is being recalled should stop distribution. Patients who have this product should contact their healthcare provider for an alternate replacement before returning the recalled product.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA See Less

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