Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,002 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,002 in last 12 months

Showing 1242112440 of 28,654 recalls

Medical DeviceJanuary 11, 2020· Cardinal Health

Recalled Item: AAMI 3 NON-REINF SURGICAL 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 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: ROYALSILK 2XLARGE Recalled by Cardinal Health Due to The gowns contain an...

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 SURGICAL GOWN XXL 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 L NS 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 SURGGWN XL LONG 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 FABRIC REINF SURG GOWN 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 NONREIN SCRBNURGOWN 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 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(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· 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· 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 3.4MM(D) X 3.8MM(P) X 6MM(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 3.4MM(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· 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 7.5MM(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· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(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
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(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 4.1MM(D) X 7.5MM(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 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 5.6MM(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