Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 24861–24880 of 28,245 recalls
Recalled Item: Secure II Med/Surg Bed Secure II and the 3002 S3 Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaTrak¿ 3500 Plus Recalled by GE OEC Medical Systems, Inc Due to GE OEC...
The Issue: GE OEC Medical Systems Inc is recalling InstaTrak¿ 3500 Plus, ENTrakTM Plus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 Med/Surg Bed Secure II and the 3002 S3 are Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra...
The Issue: Integra became aware through a complaint from a single non-US customer that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Interlink threaded lock cannula This is a locking blunt Recalled by...
The Issue: BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HT Connect Peripheral Guide Wire Part Number Description 1012587 018...
The Issue: Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 96 System Version 1.0 Software Version 2.0 Robotic Recalled by...
The Issue: This issue is only relevant for customers importing xml files into the MagNA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.0 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....
The Issue: Potential collision risk when using XVI and external beam shaping devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Desktop The EOS RT Desktop Recalled by Elekta, Inc. Due to During the...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...
The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity. Version 1.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...
The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RTP System. Used to create treatment plans for any Recalled by Elekta,...
The Issue: When bolus is present, the Effective Depth (with bolus) to the weight point...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.