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Product: Wrap

Updated: January 14, 2021 12:00 PM

Covid-19 OSHA Complaint, NORTH PACIFIC CRANE FABRICATION & HYDRAULICS, 1581 Old State Rd, CARSON, WA, 98610, USA

NORTH PACIFIC CRANE FABRICATION & HYDRAULICS, 1581 Old State Rd, CARSON, WA, 98610, USA

January 14, 2021 12:00 PM

“Location of alleged hazard(s): 1581 Old State Rd Carson, WA 98610-3110 Description of alleged hazard(s): Covid-19 Compliant- No sanitation plan or equipment for employees, or outside guests. Hazardious Chemicals- No vent or explosion proof electrical system in painting facility. Painting in undesign... See Moreated painting areas exposing employees to harsh cancer causing chemicals. Disposing of chemicals (paint, thinner, hydraulic oil and sand from wheelabrating) on property soil near wetlands. No proper drain system or holding tanks for contaminated water or oil. Black mold above office area. Exposed asbestos wrapped pipes near office.


Source: Osha.gov | Receipt Date: 2020-06-16
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Depuy Synthes Joint Reconstruction, 700 Orthopedic Drive, WARSAW, IN, 46581, USA

Depuy Synthes Joint Reconstruction, 700 Orthopedic Drive, WARSAW, IN, 46581, USA

January 13, 2021 12:00 PM

“'- There have been 6 cases of COVID in the last week. Two cases alone were in Distribution. The working conditions in Distribution are very unsanitary and unhealthy. The work stations, equipment, line totes, floors, computers, etc., are rarely ever sanitized. Food wrappers, gum, drink bottles, kleen... See Moreex, can all be found in the trash cans within the doors of shipping. No social distancing and employer does not enforce employees to wear masks. - This J - J plant is responsible for making and shipping joint replacements. The parts are constantly being handled before shipment with no regard to safety or cleanliness for the recipient.


Source: Osha.gov | Receipt Date: 2020-10-06
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Reported By SafelyHQ.com User

January 1, 2021 9:01 PM

“Company name: Precision Dose Inc.
Brand name: GUM Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 15 mL unit dose cups
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 31, 2020
Recall details: Company Announcement Precision Dose,... See MoreInc. is voluntarily recalling all lots of Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Unit Dose Cups bearing an expiration date from 1/31/2021 – 02/28/2022 (see specific lots below) to the consumer level. Precision Dose, Inc. was notified by the manufacturer of the product, Sunstar Americas, Inc., that this product may be contaminated with the bacteria Burkholderia lata.

From information provided by the manufacturer, Sunstar Americas, Inc., use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such pneumonia and bacteremia.

To date, no adverse events have been reported to Precision Dose, Inc. related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and the product impacted is:

- Distributed in cases each containing 3 shrink-wrapped plastic trays each with 10 unit dose cups, 30-pack. NDC 68094-028-62
- Distributed in cases each containing 10 shrink-wrapped plastic trays each with 10 unit dose cups, 100-pack. NDC 68094-028-61

Chlorhexidine Gluconate Oral Rinse was distributed nationwide in the USA to pharmaceutical wholesalers. Precision Dose, Inc. is notifying its consignees directly and is arranging for return of all recalled product. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact Precision Dose, Inc. at 1 (800) 397-9228 (Monday-Friday, 8:00 AM to 4:30 PM Central Time) or by email to customercare@precisiondose.com. Consumers should contact their physician or healthcare provider if they have experienced problems that may be related to using this drug product. Affected products and lot numbers follow below: AFFECTED LOTS-Chlorhexidine Gluconate Oral Rinse USP, 0.12%

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

December 28, 2020 8:00 PM

“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, I... See Morenc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 12/31/2020 – 9/30/2022 to the consumer level. This product may be contaminated with the bacteria Burkholderia lata. This is an expansion of the recall initially announced on October 27, 2020. Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia.

To date, 29 adverse events have been reported to SAI related to this recall. Affected patients tested positive for Burkholderia lata infections, typically found in sputum cultures while under treatment for other serious medical conditions. Use of the contaminated product on patients with pre-existing respiratory conditions, including those infected with Covid-19, is particularly unsafe.

The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:

- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.

The product can be identified as shown in the images below Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:

-Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 16 fl.oz. Amber Bottles. NDC #: 052376-021-02. Product Code: 1789P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022

- Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 4 fl.oz. Amber Bottles NDC #: 052376-021-04. Product Code: 1788P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. Sunstar is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Polywood, 1001 W Brooklyn St, SYRACUSE, IN, 46567, USA

Polywood, 1001 W Brooklyn St, SYRACUSE, IN, 46567, USA

December 15, 2020 12:00 PM

“Employer not enforcing social distancing Other We were not told that there have been multiple cases at Polywood. And they have been trying to keep everything under wraps.


Source: Osha.gov | Receipt Date: 2020-06-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, GIK Acoustics USA, 3731 Northcrest Rd., ATLANTA, GA, 30340, USA

GIK Acoustics USA, 3731 Northcrest Rd., ATLANTA, GA, 30340, USA

December 15, 2020 12:00 PM

“1. There are no extractor fans for ventilation, affecting the air quality. Air comes from open doors only. There is woodshop dust and fabric dust. There is an increased Covid-19 risk from lack of ventilation, compounded recently by hanging several plastic curtains to separate workstations from each... See Moreother, further reducing air circulation. 2. Employees are exposed to heat exhaustion/heat stroke hazards due to excessive indoor temperatures. 3. The employer did not monitor the level of noise in the different sectors of the plant in order to assess whether a Hearing Conservation Program was required. (CNCs, compressor, wrapping/uphosltery room, Staple guns). 4. The employer did not assess the amount of dust contaminants in the air in order to determine whether a respiratory protection program was needed. Respirator use is required, but the employer did not implement a written Respiratory Protection Program. Employees were not evaluated through medical questionnaires before wearing negative pressure respirators, and were not fit-tested. Respirators are not always provided, and replacements are not always available. 5. The masks provided for Covid-19 are not adequate and do not protect the workers. 6. Heavy materials such as pallet-loads of plywood are stored 6 to 18 feet above the floor and at times pose a hazard to those below. 7. There are no ladders on site capable of reaching the high storage shelves. Unsafe climbing by employees is the only access for less than pallet loads. 8. Electrical and pneumatic lines are hung through improvised and potentially unsafe ways. 9. Sawdust sometimes catches fire on the CNC routers despite the dust collection system, which itself poses a fire hazard. There are fire extinguishers, but they are not used for minor, smoldering fires, and they would be unable to fight a fire effectively if it got into the several hundred pounds of sawdust in the collector system.

Alleged Hazards: 9, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-10-20
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, FCA US LLC Sterling Heights Assembly Plant, 38111 Van Dyke Ave, STERLING HEIGHTS, MI, 48312, USA

FCA US LLC Sterling Heights Assembly Plant, 38111 Van Dyke Ave, STERLING HEIGHTS, MI, 48312, USA

December 3, 2020 12:00 PM

“There are many employees that are threatened by COVID19 due to social distancing inside of the plant. It is impossible to separate 6 feet on the assembly line. We are given mask that are unwrapped, we are standing in lines for 30-45 daily to get inside of the building, and we are not being tested be... See Morefore returning to work. It is very dangerous to have over 3,000 workers in a building where there isn?t real disinfectant, no testing, no social distancing, or any consistent cleaning.


Source: Osha.gov | Receipt Date: 2020-05-26
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Web Industries Inc, 3925 Ardmore Avenue, Fort Wayne, IN 46802, USA

Web Industries Inc, 3925 Ardmore Avenue, Fort Wayne, IN 46802, USA

November 10, 2020 12:00 PM

“Employees have been sick at work with symptoms of COVID-19 and were sent home, other employees have been exposed. Employees are being trained on forklifts and using forklifts after being there for two weeks. The forklift operators speed through the building. They do not stop at intersections; they d... See Morerive through without honking their horn, they have gone through intersections while employees are walking through them. Finished Goods/Shipping Department: There are individuals stacking the finished goods wrong. They are stacking piles of cloth materials unevenly. They are stacking bundles that weigh 400 to 500 pounds. They are stacking with small rolls on the bottom and large rolls on top. Bundles are stacked four to five rolls high. They are stacking them incorrectly and they are unstable. The rolls could fall over onto employees or could cause an accident. Packaging/Wrappers: The employees get up on the conveyor rollers and stand on them to pull free jammed finish wrap.


Source: Osha.gov | Receipt Date: 2020-06-23
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Reported By SafelyHQ.com User

October 28, 2020 11:00 AM

“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily... See Morerecalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 6/30/22 – 9/30/22 (see specific lots below) to the consumer level. This product may be contaminated with the bacteria Burkholderia lata.

Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia. To date, no adverse events have been reported to SAI related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:

- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.

The product can be identified by as shown in the images below: Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers are detailed in the link below.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

October 14, 2020 11:12 PM

“I bought a 4 pack of their Bakery Banana Nut Muffins. I've bought them before, so I didn't have any concerns. On opening my first one, the paper wrapper looked like it had worms on the bottom of it. I'd never seen that before, so I checked the bottom of the muffin, and that had some too. I've thrown... See Morethe rest away. As I said, I've bought these often and they've never had this, so this isn't normal. At this same location, I had gotten a pack of mini brownies in the flat plastic container and there were plastic pieces baked into the brownies. Had to throw those out too, after there were at least 5 with plastic chips in them. Clearly quality control has gone way down here. See Less
Reported By SafelyHQ.com User

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Midwest Pet Food, Inc. already recalled the following lots of Sportmix pet food products:
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- Sportmix Original Cat, 31 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 15 lb. bag. Lots: Exp 03/03/22/05/L2 | Exp 03/03/22/05/L3

Check the full outbreak announcement on fda.gov

Source: FDA
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