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Hardee's, 120 W Main St, Beulaville, NC 28518, USA
Total all time reports:
1
Latest report: April 28, 2020 12:00 PM
More incidents from:
Restaurant
Coronavirus - Covid-19
Hardee's
120, West Main Street
Beulaville
North Carolina
United States
Hardee's closes for cleaning following positive COVID-19 case
April 28, 2020 12:00 PM
“A Duplin County Hardee's was recently closed after an employee tested positive for coronavirus.
Source: wcti12.com See Less ”
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“Company name: Laboratorios Jaloma S.A. de C.V.
Brand name: Jaloma
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: August 01, 2020
Recall details: LABORATORIOS JALOMA S.A. de C.V. is voluntarily recalling all lots and all bottle sizes of the Jaloma An ... See Moretiseptic Hand Sanitizer, Ethyl Alcohol 62% With vitamin E to the consumer level. This recall has been initiated because FDA sampled the 500 mL product and found it to be contaminated with undeclared methanol (wood alcohol). Although the contamination was linked to the 500 mL product, due to the abundance of caution, Jaloma is recalling all lots of all sizes within expiry. The NDCs, lot #s, and expiration dates are listed in the table below.
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, and 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 these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.
To date, LABORATORIOS JALOMA S.A. de C.V. has not received any reports of adverse events related to this recall.
Recalled Products:
-Product(s): Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% With vitamin E
-NDCs: 65055-600-02
-Sizes: 16.9 fl oz. (1.06 pt) (500 mL)
-UPC: 7 59684 51503 3
-Lot #s & Expiration Dates: 0005295 Exp: April, 2022 / 0006373 Exp: May, 2022
-Product(s): Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% With vitamin E
-NDCs: 65055-600-01
-Sizes: 4 fl oz (120 mL)
-UPC: 7 59684 51502 6
-Lot #s & Expiration Dates: 0005412 Exp: April, 2022 / 0007134 Exp: May, 2022 / 0007834
-Exp: May, 2022 / 0009239 Exp: June, 2022
The product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The products are distributed in a 4 fl oz (120 mL) Polyethylene Terephthalate (PET) plastic bottle and a 16.9 fl oz (1.06 pt) (500 mL) PET or High-density polyethylene (HDPE) plastic bottle. Product is labeled with a red logo with the word Jaloma written in white letters. The product was distributed throughout the United States. It was imported to one (1) wholesaler and two (2) distributors.
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0007834 EXP0522
LABORATORIOS JALOMA S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release. LABORATORIOS JALOMA S.A. de C.V.is arranging for return and refund of all recalled products.
Check the full recall details on fda.gov
Source: FDA See Less ”
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Chengdu Ai Qin Colored contact lenses - recalled due to being distributed without FDA clearance, USA
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If you have received this product, immediately cease use and contact the company via online chat at www.ttdeye.com between 9AM and 6PM (GMT+8) or contact the company via email at info@ttdeye.com (24 hours) for further information.
Chengdu Ai Qin E-commerce Co., Ltd is notifying its customers by email and is arranging for return/replacement of all recalled colored contact lenses.
Chengdu Ai Qin E-commerce Co., Ltd is voluntarily recalling these contact lenses after becoming aware of the problem. Chengdu Ai Qin E-commerce Co., Ltd has notified the FDA of this action.
Check the full recall details on fda.gov
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“Company name: CME America
Brand name: BodyGuard
Product recalled: Infusion System Administration Set (infusion set)
Reason of the recall: Use of the pump system potentially could cause over-infusion or under-infusion of therapy
FDA Recall date: July 08, 2020
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This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the system or the ±13% accuracy identified in the earlier recall notification (bd.com Therefore, the use of the pump system potentially could cause over-infusion or under-infusion of therapy and patient harm. Based on those test results CME America is providing additional information and customer actions regarding its previous recall to include all infusion sets used with the BodyGuard® infusion pump distributed beginning May 2016.
CME America has defined four categories of impacted infusion sets based on delivery inaccuracy variability, two of which (Category A and B) can continue to be used in accordance with the instructions in the recall letter (bd.com CME America also announced on April 27, 2020, the decision to suspend distribution of the BodyGuard® infusion pumps and to remove all existing products from the U.S. market. CME America will work with customers to address the latest expanded infusion set recall and will continue to maintain continuity of care during the COVID-19 pandemic. Until such time that the BodyGuard® pumps have been removed from the market, CMEA will supply accessories and infusion sets in "Category A" and "Category B" to support the infusion pumps, and customers can continue to use the products in accordance with the Operator's Manual and the additional mitigations outlined in the customer letter.
Affected Product Types:
- BodyGuard BodySet
- BodyGuard Microset with Needleless Adaptor
- BodyGuard Microsets
- BodyGuard Microset w/ Non-Vented Spike Connector
- BodyGuard set with Female Luer
- BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer
- BodyGuard Microsets with Filter
- Standard BodySet with Needleless Connectors
- BodyGuard Microset with Filter and Manual Priming Valve
- CMExpress Microbore Sets
- BodyGuard Microset with Male Luer Connectors
- CMExpress Needleless Y Site Microbore Set
Check the full recall details on fda.gov
Source: FDA See Less ”
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“Company name: LIQ-E S.A. de C.V.
Brand name: Optimus
Product recalled: Hand Sanitizer
Reason of the recall: Potential Methanol Contamination
FDA Recall date: July 20, 2020
Recall details: SAN NICOLAS DE LOS GARZA, Mexico -- LIQ-E S.A. de C.V. is voluntarily recalling all lots and all bottle s ... See Moreizes of The OPTIMUS Instant Hand Sanitizer due to the potential presence of methanol (wood alcohol) that were shipped into the United States. The products were manufactured between April 27, 2020 and May 08, 2020. Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, and 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 these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, LIQ-E S.A. de C.V. has not received any reports of adverse events related to this recall.
Recalled Products: Optimus Instant Hand Sanitizer
Product(s) NDCs: 75416-002-01
Sizes: 8.5Fl Oz.(250 mL)
UPC: 7501799115621
Lot #s & Expiration Dates: (L) 20-02 EXP 05/2022
Recalled Products: Optimus Instant Hand Sanitizer
Product(s) NDCs: 75416-001-04
Sizes: 55 Gal (208 L)
UPC: 7501799118998
Lot #s & Expiration Dates: See List
Recalled Products: Optimus Instant Hand Sanitizer
Product(s) NDCs: 75416-378-04
Sizes: 1 GAL (3.78L)
UPC: 7501799118837
Lot #s & Expiration Dates: (L) 20-03 EXP 05/22
Recalled Products: Optimus Instant Hand Sanitizer
Product(s) NDCs: 75416-004-01
Sizes: 275 Gal (1,040 L)
UPC: 7501799118981
Lot #s & Expiration Dates: (L) 5200 EXP 05/2022
55 Gal Blue Drum Lot Numbers: L-1160 EXP 05/2022 ; L-2160 EXP 05/2022 ; L-3160 EXP 05/2022 ; L-1180 EXP 05/2022 ; L-2180 EXP 05/2022 ; L-2190 EXP 05/2022 ; L-1200 EXP 06/2022 ; L-2200 EXP 06/2022 ; L-3200 EXP 06/2022 ; L-4200 EXP 06/2022 ; L-5200 EXP 06/2022 ; L-1210 EXP 06/2022 L-2210 EXP 06/2022
Master Cartons Lot Numbers:
L-1150 L-2150 L-3150 L-4150 L-5150 L-6150
L-1160 L-2160 L-3160 L-4160 L-5160 L-6160
L-1170 L-2170 L-3170 L-4170 L-5170 L-1180
L-3180 L-4180 L-6180 L-1190 L-2190 L-3190
L-4190 L-5190 L-6190 L-1200 L-2200 L-3200
L-4200 L-5200 L-6200 L-2180
The Hand Sanitizer is distributed in a 55 Gal (208 L) plastic blue drum and in 8.5Fl Oz. (250 mL), 1Gal (3.78 L), and 275 Gal (1,040L) clear plastic HDPE bottles or tank. All are labeled with a green and white label. The product was distributed throughout the United States.
Each product contains a lot number consisting of a letter followed by a dash four digits (example L-1180). This number can be found on the master cartons and written in black pen on the 55 Gal blue drum and the 275 Gal plastic tank.
The individual bottles are labeled with a lot number and expiration date in the format below. See table for lot numbers of each individual bottle.
(L) 20-02 EXP 05/2022
Check the full recall details on fda.gov
Source: FDA See Less ”
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Helpful
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