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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 22141–22160 of 27,655 recalls
Recalled Item: HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product...
The Issue: A potential issue was detected that could result in blood leakage from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium VG Recalled by GE Healthcare Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique...
The Issue: The PedFuse Pedicle Screw Rod Caliper included with the MISquito Pedicle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN 3000 Series Set- Huber needles. Used in combination Recalled by...
The Issue: Needle is leaking from hub/needle cannula connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. Recalled by Merge Healthcare, Inc. Due to There is a...
The Issue: There is a potential for duplicate container numbers to be created for patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...
The Issue: The threads of the outer tube of the shock module of LP Rotate are too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS Femoral Implants Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamondback 360 Coronary Orbital Atherectomy System Recalled by...
The Issue: The OAD saline sheath outer layer may flake off from the catheter due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FLOW-i Anesthesia System Axillary O2 and Suction Module Recalled by...
The Issue: Maquet has identified that in some FLOW-i Anesthesia System Auxiliary O2 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...
The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker received four customer complaints reporting that inside the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...
The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...
The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.