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. 2,623 recalls have been distributed to Connecticut in the last 12 months.
Showing 7101–7120 of 13,380 recalls
Recalled Item: HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Recalled by...
The Issue: Superpotent and Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Naloxone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST Due to...
The Issue: Presence of Particulate Matter; Potential for particulate matter on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of assurance of sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of assurance of sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of assurance...
The Issue: Lack of assurance of sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of assurance of sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of assurance of sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluticasone propionate Nasal Spray Recalled by Apotex Inc. Due to Presence...
The Issue: Presence of foreign substance: glass particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...
The Issue: Presence of Foreign Substance: A product complaint was received for a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...
The Issue: Resuspension problems: Out of specification for appearance and resuspendability.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergan Taytulla Softgel Capsules Recalled by Allergan, PLC. Due to...
The Issue: Contraceptive Tablets Out of Sequence.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: READYFLUSH PROTECT with Dimethicone (3.2%) Recalled by Medline Industries...
The Issue: Microbial Contamination of a Non-Sterile Product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.