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The Egan Water System has been rescinded. The advisory was issued for all northside customers.
Beckley Water Co. has LIFTED the boil water advisory for 803 through 2000 C & O Dam Road including all side streets to the end of the system and including Fire Trail Drive.
22 hours ago
Charlotte Harbor Water Association has rescinded a boil water notice for its customers following a satisfactory completion of the Bacteriological survey showing the water is safe to drink.
Charlotte County Utilities Department has rescinded the boil water notice for Burnt Store Service Area customers only. The water is now safe for consumption.
City of Fairmont Water Dept. has LIFTED the boil water advisory affecting Kingmont, Airport Rd, Landing Ln, Davis St, Linn St, and the surrounding area.
19 hours ago
The recommendation to boil drinking water in the City of Tekamah has been lifted. The advisory was issued Sunday following a drop in water pressure in the city’s system following a water main break.
A boil advisory has been lifted for some Moss Bluff residents, according to Calcasieu Water Works District 1. The boil advisory was put into effect for customers on Hwy 171 between the Bronco stop and McFatter Trailer Park, and all of Old Hwy 171 following a scheduled... water outage.
The Barnesville Water Department has lifted the precautionary boil advisory due to emergency waterline repairs for service connections on East Pike St, Leggett Ave, Brill St, Dorsey Ave, Grandview St, Robinson Ave, Carl St, S Chestnut St and Sycamore St.
Recent Interesting Reports
Did my first SHEIN haul, was excited to open it, but the toxic odor coming from the products was unreal. It hit me hard, I ended up getting a headache out of the shoes especially. I had to put everything outside to air for 24 hours. I... do not know what they use to make the product, but beware especially if opening around babies or children.
The smell subsided after airing, and the products were ok to use. | Symptoms: Headache
Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary... recall only affects products with lot# GS046745. No other Clopidogrel or Atenolol products marketed by GSMS, Inc. are impacted. Both products are being recalled out of abundance of caution.
Product Description: Clopidogrel 75mg Tablets, 1,000 Count Bottle, GSMS NDC: 51407-032-10, Lot #: GS046745, Expiration Date: 12/2023
Product Description: Atenolol 25mg Tablets, 1,000 Count Bottle, GSMS NDC: 60429-027-10, Lot #: GS046745, Expiration Date: 12/2023
Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Clopidogrel is prescribed to lower the risk of having a stroke, blood clot, or serious heart problem for patients who have had heart attack, severe chest pain, or circulation problems as indicated in the product labeling. For more drug label information about clopidogrel bisulfate visit: DailyMed - CLOPIDOGREL- clopidogrel bisulfate tablet, film coated (nih.gov). For more drug label information about atenolol visit: DailyMed - ATENOLOL tablet (nih.gov)
Patients who suddenly stop taking atenolol, as would happen if clopidogrel were misplaced in the atenolol-labeled bottle, are at increased risk for ischemic (angina, myocardial infarction), hypertensive and arrhythmic adverse events relating to rapid withdrawal of beta antagonism. Further, patients who are on atenolol are frequently on concomitant anticoagulant and antiplatelet medications and would be at increased risk for bleeding if clopidogrel were added to the regimen. To date, GSMS, Inc. has not received any reports of adverse events related to the use of the products as part of this recall.
The lot under GSMS, Inc.’s voluntary recall has been primarily sold to AmerisourceBergen, and McKesson. AmerisourceBergen and McKesson are instructed to immediately stop distribution, quarantine all remaining products in their control, and return the recalled product to GSMS, Inc. They are also instructed to provide their customers, i.e., pharmacies and consumers, a copy of GSMS, Inc.’s recall notification, recall response form, and letter to consumers, patients, and caregivers.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experienced harm from these 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.
Company name: Golden State Medical Supply, Incorporated
Brand name: Golden State Medical Supply, Incorporated
Product recalled: Clopidogrel 75mg Tablets, Atenolol 25mg Tablets
Reason of the recall: Due to Label Mix-up
FDA Recall date: September 29, 2022
I received an unrequested package from 188 South Mountain House Parkway, Tracy, CA 95377.
It contained a package of tooth brushes with lettering from an Asain language I don't recognize
EMPTY BUBBLE ENVELOPE DELIVERED TO ME 1 WEEK AGO, Amazon Fulfillment Center, 1555 N Chrisman Rd, Tracy, CA, USA
4 days ago
WAS SENT A SMALL BUBBLE ENVELOPE WITH NOTHING INSIDE. WHY? USPS TRACKING # 9400 1362 0633 5671
It looks they are all hitting expiry, packets i had in the house, and have seen while shopping. Not sure if it means that they will be less reliable, or not work at all. Either way, not good timing heading into fall, where covid may flare up again.
A package delivery with "fraudulent postage applied", had to pay five dollars to get package, Amazon SJC7, 188 South Mountain House Parkway, Tracy, CA, USA
2 weeks ago
Ordered product awhile ago, paid overseas postage charge plus product price, should not have to pay $5.00 postage on something I already paid for.
My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely., Huntsville, Alabama, USA
2 weeks ago
She began to have diarrhea 3 days ago after eating the first Dream bone. We didn't relate the problem. She got a second one the next day and the diarrhea continued for 3 days. Last night blood began to pour from her. Today they are trying to see where the bleeding is coming from to save her. | Symptoms: Diarrhea, Bloody Stool
Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene, Seattle, WA, USA
2 weeks ago
Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene. Benzene is classified as a human carcinogen. Exposure to benzene can... occur by inhalation, orally, and through the skin. Depending on duration and level of exposure, it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.
Salon Tech International, Inc. has not received any reports of adverse events related to this recall. The product is used to help reduce bacteria, that potentially can cause disease, when soap and water are not available. 512 bottles of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A, Expiration 6/18/2023 was distributed in the Seattle, Washington area.
Salon Technologies International. Inc. has notified its distributors by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using and return unused product to where it was obtained.
In case you experienced 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.
Company name: Salon Technologies International Inc.
Brand name: Antica Farmacista
Product recalled: Ocean Citron Hand Sanitizer
Reason of the recall: Product contains benzene
FDA Recall date: September 19, 2022