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. 2,450 recalls have been distributed to Maine in the last 12 months.
Showing 16421–16440 of 27,655 recalls
Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Programmer Recalled by Cyberonics, Inc Due to Certain Model 3000...
The Issue: Certain Model 3000 programming events can result in miscalculation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with...
The Issue: Using different fluid formulations of NxStage PureFlow B Solution at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100...
The Issue: iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...
The Issue: An increase in the number of failed calibration events or negative bias with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...
The Issue: Certain catheters could have a compromised catheter shaft due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description Recalled by Bard...
The Issue: Specific lots of ArcticGel Pads have potential issues which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 38 Sphere Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...
The Issue: Stent length on the label may not match the length of the stent itself.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.