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.

51,038 total recalls
2,623 in last 12 months

Showing 80818100 of 51,038 recalls

Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 24, 2023· Baxter Healthcare Corporation

Recalled Item: Doxil (doxorubicin hydrochloride liposome injection) 50 mg in 25 mL (2...

The Issue: CGMP Deviations: Product was exposed to temperatures exceeding the labeled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2023· MICROVENTION INC.

Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...

The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2023· Inmar Supply Chain Solutions, LLC

Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...

The Issue: Various medical devices potentially exposed to rodent and rodent activity....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 23, 2023· Contract Pharmaceuticals Limited Canada

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Contract...

The Issue: Defective Container: slow leakage under the cap

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 23, 2023· Stryker Corporation

Recalled Item: Cinchlock SS Knotless Anchor Inserter Recalled by Stryker Corporation Due to...

The Issue: Expired Product distributed

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Knee insert...

The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Encore Medical, LP

Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...

The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Apellis Pharmaceuticals, Inc.

Recalled Item: Apellis Injection Kit 29g Injection Needle -single use intended to Recalled...

The Issue: 19-gauge x 1" inch filter needles showed appearances of a small fraction of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Qiagen GmbH

Recalled Item: therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used Recalled...

The Issue: Handbook Revision (Rev13) a dilution step is indicated as an Action when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Covidien LP

Recalled Item: Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm...

The Issue: Some catheter kits labeled as 23 cm implant length incorrectly included...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Super Rapid Readout Biological Indicator Recalled by 3M Company -...

The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...

The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Super Rapid Readout Steam Challenge Pack Recalled by 3M Company -...

The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...

The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 18, 2023· HUMANRACE

Recalled Item: Humanrace Suncare Recalled by HUMANRACE Due to Subpotent Drug: Product does...

The Issue: Subpotent Drug: Product does not contain SPF that is declared on the label.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2023· HUMANRACE

Recalled Item: Humanrace Suncare Recalled by HUMANRACE Due to Subpotent Drug: Product does...

The Issue: Subpotent Drug: Product does not contain SPF that is declared on the label.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 18, 2023· Twin City Foods, Inc.

Recalled Item: Individually Quick Frozen (IQF) Corn Recalled by Twin City Foods, Inc. Due...

The Issue: Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 18, 2023· Twin City Foods, Inc.

Recalled Item: Mixed Vegetables BEST PRICE TOPVALU Recalled by Twin City Foods, Inc. Due to...

The Issue: Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 18, 2023· Twin City Foods, Inc.

Recalled Item: Kernel Corn Recalled by Twin City Foods, Inc. Due to Potential Listeria...

The Issue: Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund