Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,464 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,464 in last 12 months

Showing 2188121900 of 50,117 recalls

Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Wrap Vest & Kilt Back-Saver Recalled by Burlington Medical, LLC...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein Panels Lipid Panel test strip: IVD Lipid Panel Recalled by...

The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...

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

Class III — Low RiskOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Quick Drop OR Apron Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Panels Lipid Panel test strip: IVD Lipid Panel Test Recalled by Polymer...

The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...

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

Class III — Low RiskOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Oversize Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Support Belt Apron Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Philips North America, LLC

Recalled Item: Philips HeartStart MRx devices in use with the M3539A AC Power Module:...

The Issue: The AC power module may fail at a higher than expected rate. If a fully...

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

Class II — Potential Health HazardOngoing
DrugJune 7, 2019· PharMEDium Services, LLC

Recalled Item: Hydromorphone HCl in 0.9% sodium chloride Recalled by PharMEDium Services,...

The Issue: Incorrect Product Formulation; Firm's customer resource center (CRC)...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 7, 2019· Akorn Inc

Recalled Item: Myorisan (isotretinoin capsules Recalled by Akorn Inc Due to Labeling: Label...

The Issue: Labeling: Label mix-up: Product secondary carton erroneously states 40mg...

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

Class III — Low RiskOngoing
Refund
DrugJune 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 100 mg TABLET BULK 90 count bottles Recalled by Teva...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis pheno-Interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q ceiling--Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q.zen biplane-Interventional Fluoroscopic X-Ray System Model...

The Issue: Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS...

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

Class II — Potential Health HazardOngoing