Illinois recalls
3,602 federal recalls affecting Illinois in the last 12 months - 390 Illinois-specific plus 3,212 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-12-17FDA-DeviceOrthofixClass IIINationwideCheck Orthofix Forza Ti Spacer labeling
Labeling contains claims that are not consistently present.
- 2025-12-17FDA-DeviceOrthofixClass IIINationwideContact Orthofix about FIREBIRD SI screw labeling
Labeling contains claims that are not consistently present.
- 2025-12-17FDA-DeviceOrthofixClass IIINationwideCheck Orthofix Pillar SA spacer labeling
Labeling contains claims that are not consistently present.
- 2025-12-17FDA-DeviceOrthofixClass IIINationwideCheck your FORZA PTC Spacer labeling
Labeling contains claims that are not consistently present.
- 2025-12-17FDA-DeviceOrthofixClass IIINationwideCheck Orthofix spacer system labeling
Labeling contains claims that are not consistently present.
- 2025-12-17FDA-DeviceBeckman CoulterClass IINationwideStop using affected Beckman Coulter reaction vessels
It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction Vessel may have a small protrusion or hair like deformity. This could cause causing instrument errors (e.g., pipetting, rake, wash carousel errors) that could delay patient results.
- 2025-12-17FDA-DeviceBardClass IINationwideStop using Bard Safe-T-Centesis drainage trays
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believe device is not yet in pleural or peritoneal space when it is, may cause discomfort, delay to treatment, injury to internal organs or vessels.
- 2025-12-17FDA-DeviceMedlineClass IINationwideCheck Medline Perfusion Syringe lot 25FMJ081
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe.
- 2025-12-17FDA-DeviceGEClass IINationwideCheck your GE Senographe Pristina mammography system
Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR ¿1020.30(j).
- 2025-12-17FDA-DevicePhilipsClass IINationwideCheck your Philips Azurion 7 M20 X-ray system
Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer. The SSD spacer is necessary to meet the FDA minimum source-skin distance requirement of 38 cm for standard fluoroscopy applications.
- 2025-12-17FDA-DeviceDraegerClass IStop using Draeger ErgoStar CM 60 connectors
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
- 2025-12-17FDA-DeviceDraegerClass IStop using Draeger ErgoStar CM 55 connectors
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
- 2025-12-17FDA-DeviceDraegerClass INationwideStop using Draeger ErgoStar CM 45 connectors
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
- 2025-12-17FDA-DeviceDraegerClass IStop using Draeger ErgoStar CM 40 connectors
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
- 2025-12-17FDA-FoodPrairie Farms DairyClass IIStop using Prairie Farms Fat Free Milk
Product may contain food-grade cleaning agents
- 2025-12-17FDA-FoodCHETAK NEW YORK LLCClass INationwideStop using Deep-brand garlic cooking cubes
Product tested positive Salmonella .
- 2025-12-17FDA-FoodCHETAK NEW YORK LLCClass INationwideDo not eat Deep-brand Pani Puri stuffing
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDon't eat Deep-brand Ponk With Tangy Sev
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDiscard Deep-brand frozen diced green mango
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideStop eating Deep-brand Premium Select Jamun
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideStop eating Deep-brand Premium Select Falsa
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideStop using Deep-brand Premium Select Turmeric
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDon't eat Deep-brand frozen green garlic
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideThrow out Deep-brand Aviyal Mix immediately
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDo not eat Deep-brand Premium Select Tapioca
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDo not eat Deep-brand frozen bottle gourd
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideStop using Deep-brand Premium Select Amla
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideThrow out Deep-brand PREMIUM Select Methi Chopped
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideThrow out Deep-brand amla slices
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideStop eating Deep-brand red guava slices
Product tested positive Salmonella .
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