Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2140121420 of 48,770 recalls

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 zee 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
Medical DeviceJune 6, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee 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 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 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
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 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 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
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
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due to...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine HCL Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL Recalled by P & L Developments, LLC Due to...

The Issue: cGMP Deviations: Firm was notified by their supplier of Cetirizine HCL Oral...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Recalled by Sun...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg/ Recalled by...

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 5, 2019· Qiagen Sciences LLC

Recalled Item: Filter-Tips Recalled by Qiagen Sciences LLC Due to Kit lots contain a small...

The Issue: Kit lots contain a small percentage of damaged Filter-Tips that are leaking...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2019· GETINGE US SALES LLC

Recalled Item: PulsioFlex Monitoring System Recalled by GETINGE US SALES LLC Due to The...

The Issue: The monitor displays an error message . The error message states "internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Inlightened Partners LLC

Recalled Item: inLight Medical LED Pads used with Polychromatic light technology system...

The Issue: LED pads with cord connectors that have v-shaped notches may not have been...

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

Class III — Low RiskOngoing
Medical DeviceJune 4, 2019· Zimmer Biomet, Inc.

Recalled Item: Ultra-Drive Irrigation Tubing Assembly Recalled by Zimmer Biomet, Inc. Due...

The Issue: The products do not have sufficient data to support the labeled shelf life...

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

Class II — Potential Health HazardOngoing