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 27441–27460 of 28,245 recalls
Recalled Item: IRISpec" CA/CB two-part urine chemistry control twin set Recalled by Iris...
The Issue: The firm recalled after it received complaints of IRISpec CA/CB two part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: Recalled...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Recalled by Sentec AG Due to SenTec is recalling a number of V-Sign"2...
The Issue: SenTec is recalling a number of V-Sign"2 Sensors due to a problem regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i Recalled by Beckman...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic...
The Issue: Baxter discovered that a Baxter technical service representative was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finapres Medical Systems Portapres with NiMh battery pack Product Usage:...
The Issue: Battery may become hot and leak
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Hemostatic Bone Putty Recalled by Synthes USA HQ, Inc. Due to...
The Issue: There is the potential for Hemostatic Bone Putty to ignite if contacted with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroCool Breathable Gown with Towels Recalled by Kimberly-Clark Corporation...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL software version 6.12 for the ABL800 analyzer. The Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aviator Drill Bit (10 mm Recalled by Stryker Spine Due to Aviator drill bits...
The Issue: Aviator drill bits are 10 mm longer than the Hybrid drill bits and are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL software version 6.12 for the ABL800 and ABL700 Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith &...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.