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. 2,492 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,492 in last 12 months

Showing 1350113520 of 27,655 recalls

Medical DeviceApril 29, 2019· Philips North America, LLC

Recalled Item: Philips Patient Information Center iX configured with a regional setting...

The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...

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

Class III — Low RiskOngoing
Medical DeviceApril 29, 2019· KaVo Dental Technologies LLC

Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...

The Issue: The sensor's look up calibration files were incorrectly programmed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Inovo, Inc

Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...

The Issue: The pressure gauge (manometer) may dislodge from the threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Cytocell Ltd.

Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...

The Issue: There is an error in the chromomap on the package insert.

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

Class III — Low RiskOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· ASTRA, LLC

Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...

The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...

The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: OR VANTEX 7FR 3L 16CM CVC ECVC6665 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PICC Line Accessory Kit CVI4285 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: NEONATAL PROCEDURE TRAY PICC CATHETERS CVI4535 Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: Neonatal Cap Change Kit DT20315 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CVC BUNDLE Recalled by Centurion Medical Products Corporation Due to Firm...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: Cap Change Kit DT20310 Recalled by Centurion Medical Products Corporation...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CVC BUNDLE MULTIMED Recalled by Centurion Medical Products Corporation Due...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355 Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing