Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 956 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
956 in last 12 months

Showing 46581–46600 of 53,829 recalls

FoodFebruary 26, 2014· Dean Foods, Inc.

Recalled Item: Lehigh Valley Dairy Farms Orange Juice FROM CONCENTRATE Recalled by Dean...

The Issue: undeclared dairy in orange juice

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 26, 2014· Dean Foods, Inc.

Recalled Item: Lehigh Valley Dairy Farms Orange Juice from concentrate HALF PINT (236 mL)...

The Issue: undeclared dairy in orange juice

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 26, 2014· Dean Foods, Inc.

Recalled Item: Swiss PREMIUM 100% Pure Orange Juice FROM CONCENTRATE Recalled by Dean...

The Issue: undeclared dairy in orange juice

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 26, 2014· HP Hood LLC

Recalled Item: my essentials brand sour cream Recalled by HP Hood LLC Due to Foreign Object...

The Issue: HP Hood LLC received one complaint of a foreign object in sour cream product...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2014· Dean Foods, Inc.

Recalled Item: Price Chopper Orange Juice Recalled by Dean Foods, Inc. Due to Undeclared Dairy

The Issue: undeclared dairy in orange juice

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 26, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...

The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT Recalled...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Apollo" Knee System: APOLLO PATELLA SZ0 28MM R Recalled by Zimmer, Inc. Due...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 Recalled by...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Apollo" Knee System: PS TIB INS SZ0/16MM APOLL PS TIB Recalled by Zimmer,...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II Constrained Knee System NKII CCK TIB INS SZ00/0-L Recalled...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: MOST Options" System (MOST) HINGED TIB INS SZ 1 16MM Recalled by Zimmer,...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II System: POLY ULTRA TIB LT SZ00/9M POLY ULTRA Recalled by...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II - Unicompartmental Knee Prosthesis: CONG TIB INS SZ1/2...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Apollo" Revision/Constrained Knee System: SZ0-16MM AK CCK TIB INSER SZ1-11MM...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿ II System ULTRA CONG INS LT SZA/9MM ULTRA CONG Recalled by...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Hospira Inc.

Recalled Item: LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet Recalled by...

The Issue: Hospira identified an incorrect lower lid (set component) had been supplied...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing