Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,395 recalls have been distributed to Idaho in the last 12 months.
Showing 24781–24800 of 27,833 recalls
Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA Recalled by Zimmer, Inc....
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRESSFIT FEM ST FX 16 X 1 Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 COCR FEMORAL HEAD (2 Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR (various sizes) Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar liners and Multipolar cups with the following dimensions in MM (38...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magna-Fx Cannulated Screw Fixation System 7.0 mm. Item codes starting...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX KEYLESS 90D X 8 and X 11 Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECON SCREW LG 5.5MM DIA and M/DN FEM IM NAIL Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 COMP PLT Recalled by Zimmer, Inc. Due to Zimmer recently conducted a...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISTAL MEDIAL FEMORAL CON Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIMTRON 6 DEG 22 HEADS Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASIA ONE-PIECE LAG SCREW Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.