Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,558 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,558 in last 12 months

Showing 1980119820 of 51,202 recalls

Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: GOWN SURG LG W/TOWEL ST BACK Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 ROYALSILK SURGGOWN BNS XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREIN SCRBNURGOWN BNS L Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONRNF SURG GWN 2XL XLNG BNS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRIC REINF SURG GOWN XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-REINF SURG GOWN LG 2 TWL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABREINF SURG GOWN LARGE Recalled by Cardinal Health Due to The gowns...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 FABRNF SCRUB SURG GWN XL NS Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 ROYALSILK SURGGOWN BNS 2XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NONREINF SURGICAL GOWN 4XL Recalled by Cardinal Health Due to The...

The Issue: The gowns contain an unknown level of bioburden, unknown microbiological...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion Assembly Pump Guts Recalled by Terumo...

The Issue: These roller pumps were assembled with pump shafts that may fail at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 4MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Roller Pump Recalled by Terumo...

The Issue: These roller pumps were assembled with pump shafts that may fail at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 6MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 3MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN¿ BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 4MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 6MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 3MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing