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. 2,024 recalls have been distributed to Illinois in the last 12 months.

55,304 total recalls
2,024 in last 12 months

Showing 2176121780 of 30,032 recalls

Medical DeviceFebruary 26, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...

The Issue: Dialyzer header leak due to possible improper torque

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...

The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm has received one report of values for patient height and weight...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...

The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· Scottcare Corporation

Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...

The Issue: The firm received a complaint of the battery exploding while recharging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader XT Product Usage: Unloader XT Extreme is an external Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: NecLoc Extrication Collar Product Usage: Necloc collars are applied to...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Miami J Collar Product Usage: Miami J collars are applied Recalled by Ossur...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Extreme Custom Product Usage: Extreme Custom is an external knee Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Purewick Corporation

Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...

The Issue: PureWick is recalling external catheter for women Wicks because the labeling...

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

Class II — Potential Health HazardOngoing