AstraLyt3_VT
astralyt3vt.bsky.social
AstraLyt3_VT
@astralyt3vt.bsky.social
AstraLyt3, or Astra, is an Alien Satellite Transmitter Rover Android. As an Exploration VTuber, her directive is to uncover Earth’s knowledge and relay it through her transmissions. She’s now working to save a vast video game archive from file corruption.
Reposted by AstraLyt3_VT
First charity event of the year !!
Streaming for Hope starting this friday 💕
COME JOIN US

WE LOVE CHARITY IN THIS HOUSEHOLD EEEE
#HFTD #Streamingforhope
January 21, 2026 at 4:55 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 1 of 1
Terra Date: 1/19/2026

Classification: Potential Foodborne Illness- Clostridium botulinum
Location: IL, IN, KY, MI, OH, WI, MD, VA, CA
Company: Tri-Union Seafoods
Brand: Genova
Product: Yellowfin Tuna

Source: FDA Recall
Tri-Union Seafoods Identifies Additional Quantities of Recalled Genova® Tuna at Limited Retailers Due to Inadvertent Distribution of Previously Recalled Product
El Segundo, CA, January 16, 2026 – Tri-Union Seafoods is cautioning consumers that a third-party distributor inadvertently released quarantined product that was associated to a February 2025 recall.…
www.fda.gov
January 20, 2026 at 3:01 PM
📡 Posting my VTuber design sheet. I cashed in my "skip the line," so tomorrow (Mon 1/19, 2pm EST) @squiiji.bsky.social will be critiquing my design live on Twitch + Youtube along with other VTubers. I'm super excited to see what Squiiji and the Shroomates come up with to help improve my design!
January 18, 2026 at 7:13 PM
I turned my flerken (cat) into rubric-chan for Squiiji3D’s discord extra credit this month. She looks good in rainbow 🌈
January 17, 2026 at 8:12 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 1 of 1
Terra Date: 1/16/2026

Classification: Device & Drug Safety- Defect
Location: Nationwide
Company: Olympus Corporation
Brand: Olympus
Product: ViziShot 2 FLEX (19G) EBUS -TBNA Needles

Source: FDA Recall
Olympus Expands Voluntary Recall for ViziShot 2 FLEX (19G) EBUS -TBNA Needles
CENTER VALLEY, Pa., (January 16, 2026) — Olympus Corporation has announced the expansion of a previous global medical device removal action for ViziShot 2 FLEX (19G) EBUS -TBNA needles (“ViziShot 2…
www.fda.gov
January 17, 2026 at 3:00 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 4 of 4
Terra Date: 1/15/2026

Classification: Potential Foodborne Illness- Salmonella
Location: Nationwide
Company: Superfoods, Inc. DBA as Live it Up
Brand: Live it Up
Product: Super Greens (Original, Wild Berry)

Source: FDA Recall
Superfoods Inc. dba Live it Up. Recalls Live it Up Super Greens Because of Possible Health Risk
Superfoods Inc. DBA as Live it Up of New York, New York is recalling all Live it Up Super Greens, including both Original and Wild Berry flavors, with lots beginning with the letter “A” and all stick…
www.fda.gov
January 16, 2026 at 3:30 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 3 of 4
Terra Date: 1/15/2026

Classification: Potential Foodborne Illness- Salmonella
Location: Nationwide
Company: Spring & Mulberry
Brand: Spring & Mulberry
Product: Multiple Flavors of Chocolate Bars

Source: FDA Recall
Spring & Mulberry Expands Voluntary Recall of Select Chocolate Bars Due to Possible Salmonella Contamination
Raleigh, North Carolina (January 14, 2026) — Spring & Mulberry is updating their press release previously issued on January 12, 2026, to expand their voluntary recall beyond Mint Leaf to include…
www.fda.gov
January 16, 2026 at 3:20 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 2 of 4
Terra Date: 1/15/2026

Classification: Potential Foodborne Illness- Listeria
Location: Nationwide
Company: The Ambriola Company
Brand: Ambriola, Locatelli, Member’s Mark, Pinna, and Boar’s Head
Product: Cheese

Source: FDA Recall buff.ly/akkdB8E
The Ambriola Company Issues Recall of Cheese Products Because of Listeria Health Risk
December 3, 2025 – The Ambriola Company is recalling select cheese products after routine testing confirmed the presence of Listeria monocytogenes, an organism which can cause serious and sometimes…
www.fda.gov
January 16, 2026 at 3:10 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 1 of 4
Terra Date: 1/15/2026

Classification: Medical Device Safety- Incorrect Low Glucose Readings
Location: Nationwide
Company: Abbott
Brand: FreeStyle Libre
Product: 3 and 3 Plus Glucose Monitoring Sensors

Source: FDA Recall
Abbott Initiates Medical Device Correction for Certain FreeStyle Libre® 3 and FreeStyle Libre 3 Plus Sensors in the U.S.
ABBOTT PARK, Ill., Nov. 24, 2025 — Abbott has initiated a medical device correction for certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors in the United States after internal testing…
www.fda.gov
January 16, 2026 at 3:00 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 4 of 4
Terra Date: 1/12/2026

Classification: Potential Foodborne Illness- Salmonella
Location: Nationwide
Company: Spring & Mulberry
Brand: Spring & Mulberry
Product: Mint Leaf Date Sweetened Chocolate Bar

Source: FDA Recall
Spring & Mulberry Issues Voluntary Recall of Mint Leaf Date Sweetened Chocolate Bar Due to Possible Salmonella Contamination
Raleigh, North Carolina (January 12, 2026) — Spring & Mulberry is voluntarily recalling lot #025255 of its Mint Leaf Date Sweetened Chocolate Bar (2.1 oz) due to possible contamination with…
www.fda.gov
January 14, 2026 at 3:30 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 3 of 4
Terra Date: 1/12/2026

Classification: Potential or Undeclared Allergen- Milk
Location: New York, New Jersey, Virginia
Company: Karison Foods & Snacks Inc
Brand: Karison
Product: Panjiri, Pinni, and Laddoo

Source: FDA Recall
Food Business Karison Foods & Snacks Inc Recalls ‘PANJIRI’, ‘ALSI PINNI’, ‘PUNJABI PINNI’, ‘BESAN LADDOO’, and ‘NO SUGAR ADDED BESAN LADDOO’ Due to Undeclared Milk Allergen
Karison Foods & Snacks Inc of Port Washington, NY 11050 is recalling 12 oz containers of ‘PANJIRI’, ‘ALSI PINNI’, ‘PUNJABI PINNI’, ‘BESAN LADDOO’, and ‘NO SUGAR ADDED BESAN LADDOO’ due to undeclared…
www.fda.gov
January 14, 2026 at 3:20 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 2 of 4
Terra Date: 1/12/2026

Classification: Potential Foodborne Illness- Botulism
Location: Nationwide
Company: Diva Fam Inc.
Brand: True Sea Moss
Product: Sea Moss Gel Superfood (various flavors 16oz glass jars)

Source: FDA Recall
Diva Fam Inc. Announces Voluntary Recall Of Sea Moss Gel Superfood Products Due to Possible Health Risk
LOS ANGELES, Jan. 9, 2026 - Diva Fam Inc. ("Diva Fam" or the "Company") today (January 9, 2026) announced a voluntary recall of all lots and flavors of Sea Moss Gel Superfood due to lack of required…
www.fda.gov
January 14, 2026 at 3:10 PM
🛰️ FDA Recall Signal Boost 🛰️
Detected Anomalies: 1 of 4
Terra Date: 1/12/2026

Classification: Potential or Undeclared Allergen- Egg and Milk
Location: Colorado
Company: VH Foods Inc. DBA Outside The Breadbox
Brand: Outside the Breadbox
Product: Bread Crumbs

Source: FDA Recall
VH Foods Inc. DBA Outside The Breadbox Issues Allergy Alert on Undeclared Egg and Milk in "Bread Crumbs"
January 12, 2026, VH Foods Inc. DBA Outside The Breadbox of Colorado Springs, CO is recalling its 8 ounce packages of "Bread Crumbs" because they may contain undeclared egg and milk
www.fda.gov
January 14, 2026 at 3:01 PM
Facial tracking test of my 3D model. Ready to submit my design to Squiiji for critique for improvements. Blendshapes were created using NEB Lite. Most of the model was made in Vroid. The dish flowers and chest radar were made in Blender. I enjoy swaying side to side to watch my antennae move 😆
January 4, 2026 at 7:04 PM