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. 2,485 recalls have been distributed to Connecticut in the last 12 months.
Showing 20421–20440 of 51,038 recalls
Recalled Item: HCG 3000U/1ML INJ in 4 mL vial Assurance Infusion (713)533-8800 Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 10MG/ FENT 1000MCG/ML INJ in 20 mL syringe Assurance Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 10MG/HYDROM 15MG/SUF 200MCG/ML INJ in 20 mL syringe Assurance Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROM 10MG/SUF 200MCG/ML INJ in 20 mL syringe Assurance Infusion Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 30MG/ MORP 8MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 35MG/MORP 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The potential exists for system movement to be permanently blocked by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Firm has received customer complaints regarding failed calibrations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT AM-05500 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE COMPONENT AN-05505 Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Maximal Barrier Drape ASK-00002-1A Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE KIT SL-05500 Recalled by Arrow International Inc Due...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow SPINAL ANESTHESIA SET ASA-25090-S Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT CK-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT YC-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.