Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,368 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,368 in last 12 months

Showing 2290122920 of 27,456 recalls

Medical DeviceJuly 28, 2014· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...

The Issue: ArjoHuntleigh received three reports where the bolt under the scale...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Becton Dickinson & Co.

Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...

The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· JK Products & Services, Inc

Recalled Item: SUN DASH RADIUS 252 PN 8000809705. The device is intended Recalled by JK...

The Issue: The integrity of the wires inside main electrical chord become compromised...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Estill Medical Technologies, Inc

Recalled Item: Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery...

The Issue: Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Galt Medical Corporation

Recalled Item: GALT VALVED TEARAWAY KIT GALT VTI w/ Sideport Stainless Steel Recalled by...

The Issue: The adhesive used in the product could dislodge when objects are inserted...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Galt Medical Corporation

Recalled Item: GALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS Recalled by Galt...

The Issue: The adhesive used in the product could dislodge when objects are inserted...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· OrthoPediatrics Corp

Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...

The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker T2 Tibia System Nail Insertion Sleeve Recalled by Stryker Howmedica...

The Issue: Stryker Orthopaedics received a report indicating some of the Nail Insertion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: 23.5 Deg Rasp Handle Assy- RIGHT Nonsterile Recalled by Zimmer, Inc. Due to...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VI DBL OFFST W/ LRG STPL Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 DBL OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Vl DBL OFFST WI LRG STPL Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: 23.5 Deg Rasp Handle Assy- LEFT Nonsterile Recalled by Zimmer, Inc. Due to...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing