Walgreens Recalls Aztreonam Infusions Due to Sterility Concerns
Walgreens Infusion Services is recalling Aztreonam 1 gram in normal saline due to a lack of sterility assurance. The affected products were distributed in six states.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a lack of sterility assurance in an infusion product, which poses a significant risk of serious injury or infection.
Plain-English summary
Walgreens Infusion Services is recalling Aztreonam 1 gram in normal saline. The recall was initiated because of a lack of sterility assurance in the product.
The affected products were distributed in Texas, Florida, Virginia, Georgia, Louisiana, and Mississippi. The recall includes all products within their expiration dates.
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Aztreonam 1 gram in normal saline
- Manufacturer
- Walgreens Infusion Services
- Category
- Drug — Infusion
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All products within expiry.
Distribution
Part of a larger recall action
This product is one of 36 recalled by Walgreens Infusion Services under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 36 products in this recall →Related recalls
Same manufacturer · Walgreens Infusion Services
See all →- SevereWalgreens Recalls IVIG Gamunex Bags Due to Sterility Concerns
FDA (Drugs) · 2016-01-06
- SevereWalgreens Recalls 0.9% Sodium Chloride/MVI Injection Bags Due to Sterility Concerns
FDA (Drugs) · 2016-01-06
- SevereWalgreens Infusion Services Recalls Dextrose and Sodium Chloride Injection Bags
FDA (Drugs) · 2016-01-06
- HighWalgreens Recalls Famotidine Injection Syringes Due to Sterility Concerns
FDA (Drugs) · 2016-01-06
- SevereWalgreens Recalls 3-in-1 TPN Formula Bags Due to Sterility Concerns
FDA (Drugs) · 2016-01-06
Same hazard · sterility failure
See all →- SevereAvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2026-09-30
- SevereAvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2026-09-30
- SevereROHTO DIGI-EYE Eye Drops Recalled Over Sterility Assurance Gap
FDA (Drugs) · 2026-07-29
- HighROHTO DRY-AID Eye Drops Recalled Due to Sterility Concerns
FDA (Drugs) · 2026-07-29
- SevereOne-Piece Introducer Tray kits recalled for sterility failure
FDA (Devices) · 2026-07-22
Similar recalls
- SevereWalgreens Recalls Thiamine Syringes Due to Sterility Concerns
FDA (Drugs) · 2016-01-06
- HighWalgreens Recalls Insulin Syringes Due to Sterility Assurance Concerns
FDA (Drugs) · 2016-01-06
- HighWalgreens Recalls Milrinone Infusion Bags Due to Sterility Concerns
FDA (Drugs) · 2016-01-06
- SevereWestern Drug Recalls Lidocaine Injection Due to Sterility Concerns
FDA (Drugs) · 2015-12-09
- SevereBaptist Health Pharmacy Recalls 1/2 Normal Saline Bags for Sterility Concerns
FDA (Drugs) · 2016-06-08
- SevereWalgreens Recalls Cefazolin Infusion Bags Due to Sterility Concerns
FDA (Drugs) · 2016-01-06