Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,994 recalls have been distributed to Arkansas in the last 12 months.
Showing 12361–12380 of 28,355 recalls
Recalled Item: AAMI 3 NON-REINF SURG GWN 3XL XLONG 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.
Recalled Item: ROYALSILK LARGE 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.
Recalled Item: AAMI 3 FABREINF SCRUB SURG GWN L 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.
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.
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.
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.
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.
Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 3MM(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.
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.
Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.