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Marijuana products cultivated by PP Wellness - recalled due to possible Aspergillus contamination, Arizona, USA

1 week ago

Arizona, United States

The Arizona Department of Health Services (ADHS) announced the recall of specific marijuana products cultivated by PP Wellness due to possible contamination with Aspergillus, a fungus that can cause allergic reactions or infection, usually in people already sick with something else. These products were sold at multiple locations with the product names listed below. To date, no illnesses have been reported.

The recalled products are:
Cultivator / Product Name / Batch Number / Product Type / Implicated Contaminant
- PP Wellness / El Alquimista / GH401 / Plant, Trim / Aspergillus
- PP Wellness / Tangie Head /GH403 / Plant, Trim / Aspergillus
- PP Wellness / Nasty Girl /GH404 / Plant, Trim / Aspergillus
- PP Wellness / The Juice / GH408/ Plant, Trim / Aspergillus
- PP Wellness / Gorilla Grapevine / GH413/ Plant, Trim / Aspergillus
- PP Wellness / The Juice / GH416 / Plant, Trim / Aspergillus

This announcement is being made out of an abundance of caution. Patients who have purchased potentially contaminated products should not ingest, inhale, or otherwise consume them and should dispose of them. Once ADHS discovered the positive test results, the establishment involved took immediate action to work with all distribution and retail partners to remove any potentially impacted products.

Aspergillus can cause allergic reactions or infections, usually in people already sick with something else. Symptoms range from asthma or cold-like symptoms to fever and chest pain among many others.

In case you experience harm from products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: azdhs.gov

65


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The recalled product is:
- TUMS Peppermint Regular Strength (500mg) tablets, packages of three rolls of 12 tablets, NPN: 01970240, Lot: HA7H, Expiry: August 2027

Company name: GlaxoSmithKline Consumer Healthcare ULC
Product recalled: TUMS Peppermint Regular Strength (500mg) tablets, packages of three rolls of 12 tablets
Reason of the recall: Due to contamination fragments of fibreglass and other material
CFIA Recall date: November 30, 2022

TUMS is an antacid indicated for adult use to relieve indigestion and heartburn caused by too much acid in the stomach. If consumed, the fragments should pass through most people's digestive systems with no concern; however, elderly people and people who have narrow areas in their intestines because of disease or surgery may be at risk of injury.

Stop using the recalled product. Follow municipal or regional guidelines on how to dispose of chemicals and other hazardous waste; or Return the product to your local pharmacy for proper disposal.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

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I received a ring,its almost like a key ring,you can squeeze it to make it tighter. It has 1 shinny clear stone and several tiny stones. I did not order this ring. It came wrapped in a plastic mailing bag,with a brown box inside, and a tiny jewelery box. See Less
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2J
anonymous8011
We also just received a package of sunglasses from them that we didn't order
-1 Reply 1 week ago
SL
anonymous8141
This same thing happened to me as well. I just received sunglasses which I did NOT order. I have called my credit card company and told them what was going on and they said I would not be charged for this. I originally ordered the table and chairs as well.
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CP
c.......r
Had you ordered something else that didn't arrive?
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KN
anonymous8087
We also just received a pair of sunglasses from them, which we never ordered.
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We also received a package of sunglasses for the that we didn't order.
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anonymous8150
I have received 2 pairs of Ray Bans that I didn't order.
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anonymous8165
We received a package of sunglasses. But not the order we sent for fire pit and chairs.
Reply 3 days ago
ST
s...........5
Same as above
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Recent Interesting Reports

Rocky Mountain Pies, LLC of Salt Lake City, Utah is recalling 31.88 oz French Silk Pie with inkjet code date 2 266, because it may contain undeclared almonds. People who have an allergy or severe sensitivity to Tree Nuts (almonds) run the risk of serious or life-threatening... See More allergic reaction if they consume these products. Red Button Vintage Creamery French Silk Pie was distributed in Arizona, Utah, Oregon, Washington, Montana, Nevada, Colorado, Wyoming, and Idaho in retail stores. No illnesses have been reported to date.

Products are packaged in a clear plastic dome and black plastic base with a “Red Button Vintage Creamery” cardboard sleeve. Recall includes only products with the inkjet code on the dome that begins with “2 266”.  Only UPC code 0 41172 81290 9 is involved in this recall.

It was discovered at a retail location by staff that cases labeled “Turtle Cream Pies” contained Turtle Cream Pies, but were labeled with the “French Silk Pie” sleeves, resulting in the undeclared allergen, as the Turtle Cream Pie contains almonds and the French Silk Pie Sleeve does not declare almonds. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's pre-operational changeover packaging process. Consumers who have purchased Red Button Vintage Creamery French Silk Pie with the Lot Code beginning with “2 266” are urged to return it to the place of purchase for a full refund.

In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Rocky Mountain Pies, LLC
Brand name: Red Button Vintage Creamery
Product recalled: French Silk Pie
Reason of the recall: Undeclared almond
FDA Recall date: November 29, 2022

Source: fda.gov
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