Product Recalls in Illinois

Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,055 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
1,055 in last 12 months

Showing 30981–31000 of 55,304 recalls

Medical DeviceJuly 26, 2017· DePuy Orthopaedics, Inc.

Recalled Item: Concorde Lift Driver Shaft AO. Used with supplemental internal spinal...

The Issue: Potential for Intra-operative breakage of driver tips

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Molnlycke Health Care, Inc

Recalled Item: 7x10" Small Utility Positioner with Cover Recalled by Molnlycke Health Care,...

The Issue: Products may not meet specifications due to possible presence of metal shavings.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 26, 2017· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...

The Issue: Presence of Particulate Matter; stainless steel

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Metabo-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: milk (Whey)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Liver-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Prostate-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Pancreas-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Thymus Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: milk (Colostrum)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Heart-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Acidophilus-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...

The Issue: Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Leci-thin-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...

The Issue: Undeclared allergens: soy (lecithin)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2017· Gold Medal Products Co

Recalled Item: CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 Recalled by Gold...

The Issue: Missing ingredient statement on the label and undeclared soy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 25, 2017· Arrow International Inc

Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...

The Issue: Finished good kits may contain incorrect components. Kits that should...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2017· Arrow International Inc

Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...

The Issue: Finished good kits may contain incorrect components. Kits that should...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2017· Siemens Medical Solutions USA, Inc.

Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...

The Issue: Siemens is releasing a letter to inform about potential data loss relevant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing