Recalled AmerisourceBergen PF Latex SG surgical gloves (size 6.5) contain powder, which can cause latex allergies and severe reactions. Stop using immediately.
Some left-handed gloves contain powder. Powdered surgical gloves are a banned medical device in the U.S. Powder on natural rubber latex gloves can aerosolize latex allergens, resulting in sensitization to latex and allergic reactions. Additional risks of powdered gloves include severe airway inflammation, conjunctivitis, dyspnea, as well as granuloma and adhesion formation when exposed to internal tissue.
AmerisourceBergen's surgical gloves (size 6.5) were recalled because some left-handed gloves contain powder. Powder can cause allergic reactions, including severe breathing issues and tissue reactions.
Powdered surgical gloves can aerosolize latex allergens, leading to sensitization and allergic reactions. This can cause severe airway inflammation, breathing difficulties, and tissue reactions if the powder comes into contact with skin or mucous membranes.
Healthcare workers and others who use these gloves for medical procedures are most at risk. Left-handed users may be affected by the powder content.
Check for the product name 'AmerisourceBergen PF Latex SG Surgical Glove', size 6.5, and item number 10112. The recall includes lot number 705366565.
Discontinue use of the recalled gloves as they contain powder that can cause allergic reactions.
No, these gloves contain powder that can cause allergic reactions, so they should not be used.
Stop using them immediately and contact AmerisourceBergen for further instructions.
Powder can aerosolize latex allergens, leading to sensitization and severe reactions like breathing difficulties and tissue inflammation.
We’ve drafted a message you can send AmerisourceBergen to request your refund or repair — edit it as you like.
Subject: Recall Z-2036-2018 — AmerisourceBergen AmerisourceBergen Hello, I own a AmerisourceBergen that is covered by recall Z-2036-2018 from AmerisourceBergen. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
