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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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WALMART SUPERCENTER, 4600 E MAIN ST, FARMINGTON, NM

Total all time reports:  10
Latest report: May 2, 2021 12:00 PM

2 employees tested positive for Covid-19

May 2, 2021 12:00 PM

“Multiple employees(2) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 05/02/2021,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

3 employees tested positive for Covid-19

December 22, 2020 12:00 PM

“Multiple employees(3) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/23/2020,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

2 employees tested positive for Covid-19

December 1, 2020 12:00 PM

“Multiple employees(2) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 12/02/2020,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

1 employees tested positive for Covid-19

November 25, 2020 12:00 PM

“An employee(1) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/25/2020,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

3 employees tested positive for Covid-19

November 10, 2020 12:00 PM

“Multiple employees(3) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/11/2020,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

An employee test positive for Covid-19

October 7, 2020 12:00 PM

“An employee(1) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19. Event Date: 10/06/2020, RR-2861

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

An employee test positive for Covid-19

September 29, 2020 12:00 PM

“An employee(1) at WALMART SUPERCENTER in FARMINGTON, NM tested positive for Covid-19. Event Date: 09/29/2020, RR-1701

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

An employee test positive for Covid-19

August 26, 2020 12:00 PM

“An employee(1) at Walmart #826 in Farmington, NM tested positive for Covid-19. Event Date: 08/26/2020

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

An employee test positive for Covid-19

August 19, 2020 12:00 PM

“An employee(1) at WALMART in FARMINGTON, NM tested positive for Covid-19.
Event Date: 08/19/2020

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

An employee test positive for Covid-19

August 12, 2020 12:00 PM

“An employee(1) at Walmart #826 in Farmington, NM tested positive for Covid-19. Event Date: August 06 Source: env.nm.gov See Less
Reported By SafelyHQ.com User

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Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. Exposure to benzene can occur through inhalation, oral, and skin.

There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans.

To date, the company has not received any reports of adverse reactions related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected bottles of hand sanitizer include a five-digit lot code printed on the bottle near the base or, in the case of the Ulta Beauty Collection product, a five-digit lot code followed by a single letter. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also attached to this notice.

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To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for these lots. 0.5% Bupivacaine Hydrochloride Injection, USP is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and obstetrical procedures. 1% Lidocaine HCl Injection, USP is indicated for the production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks when the accepted procedures for these techniques as described in standard textbooks are observed.

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- 0.5% Bupivacaine Hydrochloride Injection, USP, Single Dose Teartop Vial. NDC: Vial: 0409-1162-19 Tray: 0409-1162-02. Lot number: EG6023. Expiration Date: 01 July 2022. Strength: 0.5%, 150 mg/30 mL (5 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.
- 1% Lidocaine HCl Injection, USP Single Dose Teartop Vial. NDC: Vial: 0409-4279-16 Tray: 0409-4279-02. Lot number: EG8933. Expiration Date: 01 Aug 2022. Strength: 1%, 300 mg/30 mL (10 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.

Hospira, Inc., places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Hospira, Inc. has notified wholesalers, distributors, retailers, and hospitals by mail to arrange for return of any recalled product.

Wholesalers, distributors or retailers with an existing inventory of the lot, which is being recalled, should stop administration and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or retail level, please notify any accounts or additional locations which may have received the recalled product from you.

Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall. For additional assistance, call Stericycle at 1-800-805-3093 between the hours of 8 a.m. to 5 p.m. ET, Monday through Friday.

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