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Safety Reports: Blood

Updated:

Real Time Reports

Recall notice

Coppertone aerosol sunscreen spray products - recalled due to presence of benzene, USA

4 years ago •source fda.gov • details

Coppertone, owned by Beiersdorf, is voluntarily recalling specific lots of five Coppertone aerosol sunscreen spray products manufactured between the dates of January 10, 2021 and June 15, 2021 to the consumer level.  Coppertone has identified the presence of benzene in these lots of products Twelve lots of… See more

#recall #blood #unitedstates

Recalls Coppertone aerosol sunscreen spray products - recalled due to presence of benzene Coppertone, owned... photo #1
312   Comments Comment

Recall notice

Lilly Glucagon Emergency Kit - recalled due to loss of potency, USA

4 years ago •source fda.gov • details

Company name: Eli Lilly and Company
Brand name: Lilly
Product recalled: Glucagon Emergency Kit
Reason of the recall: Loss of potency
FDA Recall date: September 26, 2021
Recall details: Eli Lilly and Company (NYSE: LLY) is voluntarily recalling lot D239382D, Expiration April 2022, of Glucagon Emergency Kit… See more

#drugs #recall #blood #unitedstates #sub #sugar

Recalls Lilly Glucagon Emergency Kit - recalled due to loss of potency Company name: Eli Lilly and Company... photo #1
312   Comments Comment

Regulatory Report

Covid-19 OSHA Complaint, Byron Center Manor, 2115 84th St SW # A, BYRON CENTER, MI, 49315, USA

4 years ago • details

1. The employer is not following COVID protocol and is keeping positive residents in the same area as non-positive (healthy) residents. 2. The employer is not providing proper safety personal protective equipment. Employees are using one size fits all raincoats as shared gowns that are stored in… See more

#coronaviruscovid19 #osha #blood #211584thstreetsouthwest #byroncenter #michigan #unitedstates

1   Comments Comment

Regulatory Report

Covid-19 OSHA Complaint, Byron Center Manor, 2115 84th St SW # A, BYRON CENTER, MI, 49315, USA

4 years ago • details

1. The employer is not following COVID protocol and is keeping positive residents in the same area as non-positive (healthy) residents. 2. The employer is not providing proper safety personal protective equipment. Employees are using one size fits all raincoats as shared gowns that are stored in… See more

#coronaviruscovid19 #blood #osha #211584thstreetsouthwest #byroncenter #michigan #unitedstates

1   Comments Comment

Regulatory Report

Covid-19 OSHA Complaint, The American Red Cross, 700 Spring Garden St, PHILADELPHIA, PA, 19123, USA

4 years ago • details

Address located at: Philadelphia Donor Center, 700 Spring Garden Street, Philadelphia, PA 19123 Address located at: Northeast Donor Center, 1401 Rhawn Street, Philadelphia, PA 19111 Address located at: West Chester Donor Center, 523 East Gay Street, West Chester, PA 19380 Address located at: Willow Grove Donor Center,… See more

#coronaviruscovid19 #osha #blood #700springgardenstreet #philadelphia #pennsylvania #unitedstates

574   Comments Comment

Regulatory Report

Covid-19 OSHA Complaint, University Hospital, 150 Bergen Street, NEWARK, NJ, 07103, USA

4 years ago • details

Medical laboratory workers exposed to blood without proper training and PPE for bloodborne pathogens. EO 192 Complaint: Masks are not consistantly worn in lab.


Source: Osha.gov | Receipt Date: 2021-05-25

#coronaviruscovid19 #osha #blood #150bergenstreet #newark #newjersey #unitedstates

24   Comments Comment

Regulatory Report

Covid-19 OSHA Complaint, Northern NJ Donor Center, 209 Fairfield Road, FAIRFIELD, NJ, 07004, USA

4 years ago • details

1. Employees are suffering from musculoskeletal disorders due to loading and unloading blood collection equipment from the trucks and also with assisting patients on and off the tables. 2. Employees have not received adequate ergonomic training. 3. Employees utilized chemical to clean equipment and patient collection tables… See more

#coronaviruscovid19 #blood #osha #209fairfieldroad #fairfield #newjersey #unitedstates

4   Comments Comment

Recall notice

Hospira Aminosyn II, 15% - recalled due to visible particulate matter presence, USA

4 years ago •source fda.gov • details

Company name: ICU Medical, Inc.
Brand name: Hospira
Product recalled: Aminosyn II, 15%, An Amino Acid Injection, Sulfite
Reason of the recall: Presence of visible particulate matter
FDA Recall date: September 07, 2021
Recall details: ICU Medical, Inc. is voluntarily recalling one lot (2,112 units) of Aminosyn… See more

#blood #recall #drugs #unitedstates

Recalls Hospira Aminosyn II, 15% - recalled due to visible particulate matter presence Company name: ICU Med... photo #1
312   Comments Comment

Recall notice

LeadCare® Test Kits - recalled due to underestimated blood lead levels, USA

4 years ago •source fda.gov • details

Company name: Meridian Bioscience, Inc.
Brand name: Meridian Bioscience, Inc.
Product recalled: LeadCare® Test Kits
Reason of the recall: LeadCare Test Kits lots could potentially underestimate blood lead levels when processing patient blood samples
FDA Recall date: September 02, 2021
Recall details: Meridian Bioscience, Inc. (NASDAQ: VIVO),… See more

#blood #recall #medicaldevices #unitedstates

312   Comments Comment

Recall notice

Monoject Flush Prefilled Saline Syringes - recalled due to air reintroducing into the syringe, USA

4 years ago •source fda.gov • details

Company name: Cardinal Health
Brand name: Monoject
Product recalled: Flush Prefilled Saline Syringes
Reason of the recall: Products have been found to reintroduce air into the syringe after the air has been expelled
FDA Recall date: August 20, 2021
Recall details: On August 4, 2021, Cardinal Health… See more

#blood #recall #medicaldevices #unitedstates

Recalls Monoject Flush Prefilled Saline Syringes - recalled due to air reintroducing into the syringe Compan... photo #1
312   Comments Comment

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