Walgreens, 2350 East Market Street, YORK, PA, 17402, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
1. The employer has not implemented a COVID-19 prevention program including good housekeeping practices of regularly cleaning and disinfecting surfaces, equipment, and other elements of the work environment.
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2022-01-10
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2022-01-10
121
Recent Interesting Reports
Received item I did not order, 70 Gibson Drive, Markham, Ontario, Canada
3 weeks ago •reported by user-qnbwc752
So I just randomly received a Honda keychain that I DID NOT order because I DO NOT drive at all. This is weird to me and I see I am definitely not the only person who received randomness from this address. Answers?
189
Unordered bare naturals bio ribose, Amarillo, TX, USA
4 weeks ago •reported by user-mrhd1868
I got a package in the mail and did not order it. it came from the fullfillment center in florida. contained was a small tub of white powder? bare naturals bio ribose? not sure if this is legit or not so it went in the trash .
but this worries me people are sending unordered stuff to an address i never gave out .
116
Empty package, Fishing Creek, MD, USA
1 week ago •reported by user-gnxv8262
Received empty package with sender name of Emily hunt 125 Jackson ave Edison NJ 08837
1
I received two packages of Verti Bioribose that I have not ordered, Naples, FL, USA
2 weeks ago •reported by user-bkqwv767
I have not ordered this product.
120
Received a ring that I didn’t purchase!, Arizona, USA
2 weeks ago •reported by user-qpzz3148
I’m in Arizona and I received a ring from a place called Yoshi Deals 44211 Yucca Ave. Lancaster Ca 93534. I did not order this ring!
105
Unordered Package, Albany, NY, USA
1 day ago •reported by user-gwxcb771
A small package was delivered to me with a purple plastic bottle inside. Was labeled but all in Chinese. Bottle half filled with unknown liquid. Did not order and not sure where came from.
142
I ordered a sweatshirt and got a amarata jacket, Bucuresti ,str Aleea Lunca Siretului,nr 1A,sector 6
3 weeks ago •reported by user-ydfg4319
I got a jacket and I ordered a trnind
Veteran Hand Crafts Facebook Scam, 9208 Charles Smith Ave, Rancho Cucamonga, CA 91730, USA
2 weeks ago •reported by user-rttc3191
Ordered on March 24th supposed to be a sun catcher of cardinal on glass. Got a picture on plastic that was 6x8!!!! Paid 30.95 for this -Also its a DISGRACE that they use the veterans to get their business. this has got to stop !!!!!!!!!!! this is
a scam that is being reported to the BBB-its a disgrace that they used our veterans this way.
Jerry(001)-YASF****
Jerry(001)-YASF****
703
Dr. Reddy’s Sapropterin Dihydrochloride Powder for Oral Solution - recalled due to decreased potency, USA
2 days ago •source www.fda.gov
Recall notice
Dr. Reddy's Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as "Dr. Reddy's"), today announced that it is voluntarily recalling six (6) lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg to the consumer level due to
powder discoloration in some packets leading to decreased potency. The issue was discovered during an accelerated stability test in addition to customer complaints. Sapropterin Dihydrochloride Powder for Oral Solution 100 mg was distributed nationwide to wholesalers/retailers. Dr. Reddy’s Laboratories Inc. has not received any reports of adverse events related to this recall to date.
Reduced efficacy of the product would result in elevated Phenylalaninemia (Phe) levels in patients. Chronically elevated Phe levels in infants and children are likely to cause permanent neurocognitive deficits, including permanent and irreversible intellectual disability, developmental delay, and seizures. Furthermore, elevated Phe levels during pregnancy, especially in early gestation, are associated with microcephaly and congenital heart disease.
The product is indicated to reduce blood phenylalanine (Phe) levels in adult and pediatric patients one month of age and older with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin-(BH4-) responsive Phenylketonuria (PKU) and is packaged in individual packets, 30 per carton. The affected Sapropterin Dihydrochloride Powder for Oral Solution 100mg lots include the following:
- Product Name: Javygtor™ (Sapropterin) Dihydrochloride) Powder for Oral Solution 100 mg, Lot Number: T2202812; T2204053; T2300975; T2300976; T2304356, Expiration date: 07/2025; 10/2025; 02/2026; 02/2026; 08/2026, NDC Number: 43598-097-30; 43598-097-30; 43598-097-30; 43598-097-30; 43598-097-30
- Product Name: Sapropterin Dihydrochloride Powder for Oral Solution 100 mg, Lot Number: T2200352, Expiration date: 12/2024, NDC Number: 43598-477-30
Dr. Reddy’s Laboratories Inc. is notifying its distributors and customers by recall notification letters and is arranging for returns of all recalled products. Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Consumers who have Sapropterin Dihydrochloride Powder for Oral Solution 100 mg which is being recalled should contact their physician before stopping use of the product. Consumers who have Sapropterin Dihydrochloride Powder for Oral Solution 100 mg which is being recalled should return it to their place of purchase.
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.
Company name: Dr. Reddy’s Laboratories Inc
Brand name: Dr. Reddy’s
Product recalled: Sapropterin Dihydrochloride Powder for Oral Solution 100 mg
Reason of the recall: Decreased Potency
FDA Recall date: April 23, 2024
Source: www.fda.gov
Reduced efficacy of the product would result in elevated Phenylalaninemia (Phe) levels in patients. Chronically elevated Phe levels in infants and children are likely to cause permanent neurocognitive deficits, including permanent and irreversible intellectual disability, developmental delay, and seizures. Furthermore, elevated Phe levels during pregnancy, especially in early gestation, are associated with microcephaly and congenital heart disease.
The product is indicated to reduce blood phenylalanine (Phe) levels in adult and pediatric patients one month of age and older with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin-(BH4-) responsive Phenylketonuria (PKU) and is packaged in individual packets, 30 per carton. The affected Sapropterin Dihydrochloride Powder for Oral Solution 100mg lots include the following:
- Product Name: Javygtor™ (Sapropterin) Dihydrochloride) Powder for Oral Solution 100 mg, Lot Number: T2202812; T2204053; T2300975; T2300976; T2304356, Expiration date: 07/2025; 10/2025; 02/2026; 02/2026; 08/2026, NDC Number: 43598-097-30; 43598-097-30; 43598-097-30; 43598-097-30; 43598-097-30
- Product Name: Sapropterin Dihydrochloride Powder for Oral Solution 100 mg, Lot Number: T2200352, Expiration date: 12/2024, NDC Number: 43598-477-30
Dr. Reddy’s Laboratories Inc. is notifying its distributors and customers by recall notification letters and is arranging for returns of all recalled products. Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Consumers who have Sapropterin Dihydrochloride Powder for Oral Solution 100 mg which is being recalled should contact their physician before stopping use of the product. Consumers who have Sapropterin Dihydrochloride Powder for Oral Solution 100 mg which is being recalled should return it to their place of purchase.
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.
Company name: Dr. Reddy’s Laboratories Inc
Brand name: Dr. Reddy’s
Product recalled: Sapropterin Dihydrochloride Powder for Oral Solution 100 mg
Reason of the recall: Decreased Potency
FDA Recall date: April 23, 2024
Source: www.fda.gov
303
Unordered “Keto Pure”, Oneonta, NY, USA
3 days ago •reported by user-xjtwr681
Received package today with a bottle of pills. I definitely did not order them.
Three fraud charges on my card and I had to cancel card. Will I continue to get these charges?
Three fraud charges on my card and I had to cancel card. Will I continue to get these charges?
29
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