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 27241–27260 of 28,245 recalls
Recalled Item: MX 16-slice CT Scanner System Recalled by Philips Medical Systems...
The Issue: On August 24, 2012 the firm recalled the MX 16-slice after discovering that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...
The Issue: King Systems received a customer complaint indicating that the customer had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...
The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...
The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...
The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...
The Issue: Modular necks were manufactured out of specification by a vendor; the taper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...
The Issue: During regular product monitoring, Siemens has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Discs Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the product because the cartridges may contain discs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...
The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: The firm is recalling the product due to some cartridges may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam 4.1. Radiation treatment planning software designed...
The Issue: During the planning process the beam weights can be changed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...
The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...
The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.