Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,609 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,609 in last 12 months

Showing 1030110320 of 28,641 recalls

Medical DeviceJanuary 13, 2021· Medical Components, Inc dba MedComp

Recalled Item: Power Injectable CT Port insertion kits - Product Usage: is Recalled by...

The Issue: The 5F Dignity CT Port kits were packaged with the incorrect size port. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2021· Shent USA, Inc.

Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling

The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2021· Shent USA, Inc.

Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling

The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2021· Natus Manufacturing Limited

Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...

The Issue: The external drainage system failed to meet Pyrogen test requirements for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· C.R. Bard, Inc.

Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...

The Issue: The device catheter tip was cut off (no tip) and the product packaging was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Ecolab Inc

Recalled Item: Slush + Warmer Disc Drape Recalled by Ecolab Inc Due to Slits were...

The Issue: Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2021· Nihon Kohden America Inc

Recalled Item: WMTS Telemetry Receiver Recalled by Nihon Kohden America Inc Due to...

The Issue: Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2021· Cairn Diagnostics

Recalled Item: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended...

The Issue: Potential for false negative diagnosis of gastroparesis. Certain GEBT kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2021· DePuy Orthopaedics, Inc.

Recalled Item: Universal Femoral Sleeves - Product Usage: used primarily in revision...

The Issue: The taper dimensions may be out of specification due to a production issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Kendall Blue L Recalled by Cardinal Health 200, LLC Due to Foreign...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: CHEMOPLUS DRUG SPILL KIT HOS Recalled by Cardinal Health 200, LLC Due to...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Kendall Spill Kit Recalled by Cardinal Health 200, LLC Due to Foreign Object...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS 2X-Large White Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS 2X-Large Blue Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS Medium White Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: ChemoPlus" Chemo Prep & Admin Kit Recalled by Cardinal Health 200, LLC Due...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Isolation W/Ties Univ Ylw Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing