Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,486 recalls have been distributed to Wyoming in the last 12 months.
Showing 16361–16380 of 27,462 recalls
Recalled Item: CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR SIZE 0 STD prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...
The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...
The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...
The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...
The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...
The Issue: It was discovered that the product units it imported may, at peak levels,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...
The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...
The Issue: Potential for positional errors following automatic table movement (ATM).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...
The Issue: When calculating electron Monte Carlo dose with a very large number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...
The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Pump Recalled by CareFusion 303, Inc. Due to The syringe plunger...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to The syringe...
The Issue: The syringe plunger grippers may fail to automatically close around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.