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[Recalled] PopLok Punch labeled in part: "PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere, FINLAND***Rx Only***ConMed Linvatec 11311 Concept Blvd Largo, FL 33773-4908 USA***Made in

FDA recall notice for PopLok Punch labeled in part: "PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere

[Recalled] Strawberry, 1pt., UPC 8 52244 00305 3 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Strawberry, 1pt., UPC 8 52244 00305 3 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2012-07-06.

[Recalled] Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 41130-21663, Distributed by Supervalu Inc, Eden Prairie, MN 55344. SunnyBr

FDA recall notice for Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bon Bon Light Ice Cream, Half Gallon (1

[Recalled] Chocolate Dipped Bars, 2 Chocolate & 2 Vanilla, 2.1 fl oz bars, UPC 8 52244 00308 4 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Chocolate Dipped Bars, 2 Chocolate & 2 Vanilla, 2.1 fl oz bars, UPC 8 52244 00308 4 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2

[Recalled] Chocolate, 1pt., UPC 8 52244 00300 8 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Chocolate, 1pt., UPC 8 52244 00300 8 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2012-07-06.

[Recalled] Coffee, 1pt., UPC 8 52244 00302 2 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Coffee, 1pt., UPC 8 52244 00302 2 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2012-07-06.

[Recalled] Vanilla Maple, 1pt., UPC 8 52244 00306 0 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Vanilla Maple, 1pt., UPC 8 52244 00306 0 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2012-07-06.

[Recalled] Pumpkin Spice, 1pt., UPC 8 52244 00307 7 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Pumpkin Spice, 1pt., UPC 8 52244 00307 7 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2012-07-06.

[Recalled] Chocolate Peanut Butter, 1pt., UPC 8 52244 00301 5 — Arctic Zero Inc | FDA 2012-07-06

FDA recall notice for Chocolate Peanut Butter, 1pt., UPC 8 52244 00301 5 (Arctic Zero, Inc.). Reason: Arctic Zero Inc. Issued 2012-07-06.

[Recalled] ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is a sterile, single use, surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and

FDA recall notice for ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is a sterile, single use, surgical gown intended to protect surgical

[Recalled] The ABL software version 6.12 for the ABL800 and ABL700 analyzer. The analyzers are intended for the in Vitro testing of: -Samples of whole blood for the parameters pH, pO2, pCO2, cK+, cNa+, cCa2+, cCl-, cGlu, cLac, cCrea, ctB

FDA recall notice for The ABL software version 6.12 for the ABL800 and ABL700 analyzer. The analyzers are intended for the in Vitro testing of: -Samples of wh

[Recalled] ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer is intended for in vitro testing of samples of heparinized whole blood. — A customer has reported an error on an ABL8xx configured to a Hospital Informat… | FDA 2012-0

FDA recall notice for ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer is intended for in vitro testing of samples of heparinized whole blood. (Rad

[Recalled] MicroCool Breathable Gown with Towels, X-Larg, X-Long, Sterile The product is a sterile, single use, surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fl

FDA recall notice for MicroCool Breathable Gown with Towels, X-Larg, X-Long, Sterile The product is a sterile, single use, surgical gown intended to protect

[Recalled] Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and VB1025.10S. Indicated for use as a water soluble implant material and for use in the control of bleeding from bone

FDA recall notice for Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and VB1025.10S. Indicated f

[Recalled] Twist'n Sparkle Home Beverage Carbonation System plastic bottles. — The products are plastic bottles used as a part of the iSi Twist'n Sparkle Beve… | CPSC 2012-07-05

CPSC recall notice for Twist'n Sparkle Home Beverage Carbonation System plastic bottles.. Reason: The products are plastic bottles used as a part of the iSi Twi

[Recalled] Soy Candles — The candles are 7.5 oz | CPSC 2012-07-05

CPSC recall notice for Soy Candles (Bath Petals Inc., of Gardena, Calif.). Reason: The candles are 7.5 oz. Issued 2012-07-05.

[Recalled] Great American Seafood Imports Co. Cooked Shrimp Meat. Size: 300/500 count per pound in 2-lb (item #06834) and 5-lb (Item #07756) packages. — Southwind is recalling cooked shrimp meat because it contains undeclared red #4… | FDA

FDA recall notice for Great American Seafood Imports Co. Cooked Shrimp Meat. Size: 300/500 count per pound in 2-lb (item #06834) and 5-lb (Item #07756) package

[Recalled] Flavored coffee. Cafe Moto Almond Truffle Flavored Coffee, 16 oz. — The recall was initiated because the Almond Truffle flavoring used in the manuf… | FDA 2012-07-05

FDA recall notice for Flavored coffee. Cafe Moto Almond Truffle Flavored Coffee, 16 oz. (Cafe Moto). Reason: The recall was initiated because the Almond Truffle

[Recalled] Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures (COBRAID-blue, COBRAIDblack), sterile Part Number: 72202896 Product Usage: intended for use for the reattachment of soft tissue to bone — Distal part of the

FDA recall notice for Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures (COBRAID-blue, COBRAIDblack), sterile Part Number: 72202896 Product

[Recalled] Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), sterile Part Number: 72202895 Product Usage: intended for use for the reattachment of soft tissue to bone — Distal part of the anchor m

FDA recall notice for Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), sterile Part Number: 72202895 Product Usage: