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Abbott Powder Infant Formula - recalled due to Cronobacter & Salmonella, USA

2 years ago •source www.fda.gov

Recall notice

Abbott Powder Infant Formula - recalled due to Cronobacter & Salmonella photo #1

United States

*Update* March 07, 2022
EXPANDED: Abbott is voluntarily recalling one lot of Similac PM 60/40 (Lot # 27032K80 (can) / Lot # 27032K800 (case)) manufactured in Sturgis, Michigan. This is in addition to lots of Similac®, Alimentum® and EleCare® powder formula that were voluntarily recalled on Feb. 17. The action comes after learning of the death of an infant who tested positive for Cronobacter sakazakii and who we were informed had consumed Similac PM 60/40 from this lot. This case is under investigation, and at this time the cause of the infant’s Cronobacter sakazakii infection has not been determined.

Feb 17th, 2022
The FDA announced the recall of Abbott powder formulas, including Similac, Alimentum and EleCare manufactured in Sturgis, Mich., one of the company's manufacturing facilities. The recall does not include any metabolic deficiency nutrition formulas.

Abbott is voluntarily recalling these products after four consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants who had consumed powder infant formula manufactured in this facility. Additionally, they conduct routine testing for Cronobacter sakazakii and other pathogens in our manufacturing facilities. During testing in Sturgis, Mich., facility, they found evidence of Cronobacter sakazakii in the plant in non-product contact areas. They found no evidence of Salmonella Newport. This investigation is ongoing.

Importantly, no distributed product has tested positive for the presence of either of these bacteria, and we continue to test. All finished products are tested for Cronobacter sakazakii, Salmonella Newport and other pathogens and they must test negative before any product is released. Additionally, retained samples related to the three complaints for Cronobacter sakazakii tested negative for Cronobacter sakazakii. And the retained sample related to the complaint for Salmonella Newport tested negative for Salmonella Newport.

While Abbott's testing of finished product detected no pathogens, they recalled the powder formula manufactured in this facility with an expiration of April 1, 2022, or later. No Abbott liquid formulas, or nutrition products from other facilities are impacted by the recall.

Cronobacter sakazakii is commonly found in the environment and a variety of areas in the home. It can cause fever, poor feeding, excessive crying or low energy as well as other serious symptoms. It's important to follow the instructions for proper preparation, handling and storage of powder formulas.

What parents and caregivers should do: the products under recall have a multidigit number on the bottom of the container starting with the first two digits 22 through 37, contains K8, SH, or Z2 and with an expiration date of April 1, 2022, or after. To find out if the product you have is included in this recall, check the link below. Some product was distributed to countries outside the U.S.

Company name: Abbott
Brand name: Similac, Alimentum, and EleCare
Product recalled: Powder Infant Formula
Reason of the recall: Consumer complaints regarding Cronobacter sakazakii, Salmonella Newport.
FDA Recall date: February 17, 2022

Check the full recall details on www.fda.gov

Source: FDA

#recall #babyformula #us #salmonella #salmon #actii

303 2 Shares

Recent Interesting Reports

Medline and Centurion Convenience kits - recalled due to lack of sterility, USA

3 weeks ago •source www.fda.gov

Recall notice

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium … See More
Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

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: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024

Source: www.fda.gov
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#recall #medicaldevices #us

Medline and Centurion Convenience kits - recalled due to lack of sterility photo #1
303
C

Unordered Package, Groveland, MA, USA

1 week ago •reported by user-cnkv6673

I received a bottle of detox daily detox slim fitfusion I did not order this I don't know how they got my address I better not be charged I just had to change my debit card because someone stole it so I'm sure that this has something … See More
to do with that how do I send it back I better not be getting charged
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#unorderedpackage #groveland #massachusetts #us

Unordered Package photo #1
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I bought Daisy by Marc Jacobs from Amazon and it was FAKE!!!, Greenwood, LA, USA

3 weeks ago •reported by user-pwgt4515

I bought Daisy by Marc Jacobs from Amazon and it was FAKE!!! I went and looked at the other perfume I have bought also and to my HORROR THOSE ARE FAKES AS WELL!!! BEWARE!!!
I checked my perfume that I paid a lot of money for from … See More
Amazon and it was a fake and upon checking my other perfume.. they are all fake!!!  | Symptoms: Other
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#falseadvertising #amazon #greenwood #louisiana #us

I bought Daisy by Marc Jacobs from Amazon and it was FAKE!!! photo #1
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