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. 2,451 recalls have been distributed to Arkansas in the last 12 months.
Showing 28161–28180 of 28,355 recalls
Recalled Item: 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 Neck Taper 00789503201 VerSys Femoral Head Provisional 32mm -3.5...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 Neck Taper 00789504001 VerSys Femoral Head Provisional 40mm -3.5...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When performing a...
The Issue: When performing a secondary capture generated from GSI Viewer, the header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant...
The Issue: Stryker Spine has received six reports regarding the breakage of one or more...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to May go to a white...
The Issue: May go to a white screen due to a problem with the SOM2 module. A white...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to May go to a white...
The Issue: May go to a white screen due to a problem with the SOM2 module. A white...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces...
The Issue: Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imagecast PACS is an image management system intended to be Recalled by Ge...
The Issue: In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ****** 3mm Diamond Ball. Used for cutting and shaping bone. Recalled by The...
The Issue: Due to three batches of product may have diamond grit size larger than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.