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 26601–26620 of 51,038 recalls
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNI-CP Recalled by NewDeal SA Due to Use of the impacted product may cause a...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your 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: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...
The Issue: The block used to connect the patient pallet to the couch may be assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Melanie Mini Cookies with Caramel Flavor in a 17.6 oz Recalled by Desly...
The Issue: Products contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Broccoli cuts Recalled by Ahold USA Due to Potential Listeria Contamination
The Issue: Ahold Delhaize received a report from State of CT of finding significant...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic Recalled by...
The Issue: Products contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...
The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...
The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...
The Issue: Potential for control line not appearing on the test strip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziyad Brand Tahini Recalled by Ziyad Brothers Importing, Inc. Due to...
The Issue: Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
Recalled Item: screamin' hot (capsaicin) Pain Relieving Gel Recalled by Ideaz Llc Due to...
The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.