Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
34,894 found- Use cautionDrug
PharMEDium Services, LLC. recalls Hydromorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Injection 1 mL, packaged in syringes, Rx Only , PharMEDium
PharMEDium recalls 0.5 mg/mL hydromorphone injections due to potency errors. This may cause overdose risks. Check NDC 61553-352-40 and lot number 172820134M.
PharMEDiumOct 13, 2017 - Lower riskDrug
Sanofi-Aventis U.S. LLC recalls Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The
Sanofi recalls Clolar injection vials (20 mg/20 mL) because they lack the correct package insert for brand-name clofarabine. This affects authorized generic products.
SanofiOct 13, 2017 - Lower riskFood
ASK Foods Inc recalls taste of Inspirations Classic Red Skin Potato Salad; Net Wt. 16 oz.,; Sell By: 10-20-2017 (top label). taste of
ASK Foods is recalling a lot of Classic Red Skin Potato Salad (16 oz) sold by Hannaford Supermarkets that may contain undeclared egg. Consumers should check labels for the specific sell-by date and contact the company for details.
ASK FoodsOct 13, 2017 - Lower riskFood
Whole Foods Market recalls Whole Foods Hand Pie Apple Cinnamon 3 PK, NET WT 8 oz. PLU number 23646100000
Whole Foods Market recalls 3-pack apple cinnamon hand pies with undeclared egg allergen. Consumers should check best-by dates (Oct 15, 2017 or earlier) and avoid if allergic to egg.
Whole Foods MarketOct 13, 2017 - Lower riskFood
FLAVORx Inc. recalls FLAVORx Sweetening Enhancer , the product is packaged as follows: Fillmaster Auto Sweetening Enhancer AQ, 4oz Bottle,
FLAVORx recalls Sweetening Enhancer bottles with microbial growth detected in stability testing. Products sold between 2018-2019 may pose health risks. Consumers should check lot numbers and contact FLAVORx for details.
FLAVORxOct 13, 2017 - Lower riskFood
Wegmans Food Markets, Inc. recalls 033710 - Wegmans Puff Fruit Dumplings, 2 Pack, 6 oz. UPC: 0 77890 33710 3
Wegmans recalls 2-packs of Puff Fruit Dumplings due to undeclared FD&C Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup. Consumers should check UPC 077890337103 and lot dates through 10/15/2017.
WegmansOct 13, 2017 - Lower riskFood
San Gennaro Foods, Inc recalls Traditional Polenta, San Gennaro brand, Pre-cooked Ready to Heat & Serve, 12/18 oz packages, UPC# 7-62676-15000-6
San Gennaro Foods recalls polenta products with unapproved food contact ink that could pose health risks. Affected items include 12/18oz and 6/18oz packages with specific UPC codes.
San GennaroOct 13, 2017 - Use cautionConsumer product
Macy's Recalls Martha Stewart Whiteware Cake Knife and Server Sets Due to Laceration Hazard
Macy's recalls Martha Stewart Whiteware cake knife and server sets due to handle breakage causing lacerations. Affected items have white ceramic handles with 'Martha Stewart Collection' embossing and specific UPCs.
Macy'sOct 13, 2017 - Stop using nowMeat & poultry
J & B Sausage Company, Inc. Recalls Fully Cooked Shredded Beef Products Due To Possible Foreign Matter Contamination
J Bar B Foods recalls 12,816 pounds of fully cooked shredded beef products from Sept. 16, 2017, that may contain plastic. Consumers are urged not to consume these items.
J Bar B FoodsOct 12, 2017 - Use cautionMedical device
Covidien LLC recalls Situate Gauze RF and X-Ray detectable. Product Number: G0804-16P02CN-1 Situate premium cotton are single use cotton
Covidien recalls Situate Gauze RF and X-Ray detectable products due to potential failure to detect by the Situate console from a manufacturing error. Affected items have Product Number G0804-16P02CN-1 and Lot Number 170704A.
CovidienOct 12, 2017 - Lower riskDrug
Genzyme Corporation recalls Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection, for intravenous use, Rx Only, Mfd. by: Teva Pharmachemie Swensweg
Genzyme recalls Clolar (clofarabine) 20 mg/20 mL injections due to incorrect or missing package inserts. Patients should contact their doctor for guidance.
GenzymeOct 12, 2017 - Use cautionDrug
Hetero Labs, Ltd. - Unit III recalls Levetiracetam Oral Solution, USP, 100 mg/mL, packaged in a 16 fl oz (473 mL) bottle, Rx only, Manufactured for: Camber
Hetero Labs recalls Levetiracetam Oral Solution (100 mg/mL) due to a foreign screw in the bottle. This could cause injury if the bottle breaks. Contact the manufacturer for details.
Hetero LabsOct 12, 2017 - Lower riskFood
Slade Gorton & Company, Inc. recalls Icybay Brand Frog Legs, 4/6 Ct / Lb Farm Raised Trimmed, Frozen. 30 lb. Master Carton (5 lb. inner boxes 6 boxes per
Slade Gorton & Company recalls Icybay Brand Frog Legs due to unapproved antibiotics (nitrofurans and chloramphenicol) in frozen product. Consumers should check UPC codes 073129282770 and PC # 28277 for affected items.
IcybayOct 12, 2017 - Use cautionVehicle
FOREST RIVER VENGEANCE (2018) recall — Electrical System
Forest River recalls 2017-2018 Vengeance trailers with generator exhaust too close to underbelly, risking fire. Owners must have exhaust pipe lowered to prevent fire.
Forest RiverOct 11, 2017 - Use cautionVehicle
DYNAMAX ISATA (2018) recall — Engine And Engine Cooling
Forest River recalls 2017-2018 Dynamax Isata vehicles with leaking water pumps that could cause engine compartment fires. Owners must have water pumps replaced free by dealers.
Forest RiverOct 11, 2017 - Lower riskMedical device
Biomerieux Inc recalls VITEK2 GP-ID, REF 21342 IVD
Biomerieux recalls VITEK2 GP-ID ID cards due to atypical negative reactions for Enterococcus casseliflavus, risking false negative QC test results. Affected lots include specific UDI and lot numbers.
BiomerieuxOct 11, 2017 - Use cautionMedical device
GE Medical Systems China Co., Ltd. recalls Carestation 620 A2, Carestation 650 A2, and Carestation 650c A2
GE Medical recalls Carestation 620 A2, 650 A2, and 650c A2 models with possible CO2 leak risk. Affected units have specific serial numbers and model codes.
GE MedicalOct 11, 2017 - Use cautionMedical device
Spacelabs Healthcare, Ltd. recalls Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The
Spacelabs recalls Arkon anesthesia workstations with software version 2.61 due to potential mechanical ventilation failure and blank display without alarms. Affected units may need repair or software update.
SpacelabsOct 11, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: To provide fixation of soft tissue grafts within the
Zimmer Biomet recalls TunneLoc Tibial Fixation Devices in ACL kits due to potential inadequate sterilization. This may affect surgical implants used in ACL/PCL reconstruction procedures.
Zimmer BiometOct 11, 2017 - Use cautionMedical device
Zimmer Dental Inc recalls Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the product is Manufactured by Zimmer Dental Inc., Carlsbad,
Zimmer Dental recalls GemLock RHD2.5 Hex Drivers due to potential failure to engage dental implant fixtures, risking improper implant placement. Affected lot numbers: 63563072, 63572755, 63583270, 63755802.
Zimmer DentalOct 11, 2017 - Lower riskFood
Pacific Foods of Oregon, Inc. recalls SKU 57879, Trader Joe's Organic Tomato & Roasted Red Pepper Soup, packaged in a Tetra Pak aseptic container/carton.
Pacific Foods of Oregon recalls Trader Joe's Organic Tomato & Roasted Red Pepper Soup due to potential under processing. Consumers should check for specific batch codes and contact the manufacturer for details.
Pacific Foods of OregonOct 11, 2017 - Lower riskFood
Kenny's Great Pies, Inc. recalls Kenny's Buckeye Pie, Net Wt.22 oz. (624g).
Kenny's Great Pies recalls 22oz Buckeye Pie with undeclared wheat. Consumers should check UPC codes 7 11276 50277 7 and lot dates 8/22/2017 to 9/27/2017 for affected products.
Kenny's Great PiesOct 11, 2017 - Use cautionVehicle
CHRYSLER 200 (2013) recall — Seats
Chrysler recalls 2013 200 models with potential seat headrest failure during rear-end crashes. Owners must contact FCA for free ORC replacement.
ChryslerOct 10, 2017 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or
ImplantDirect Legacy 3 Implant (13mm L, REF 864713) recalled due to potential sterilization compromise from improper cap sealing. Affected units sold with lot number 79607.
ImplantDirectOct 10, 2017 - Lower riskMedical device
Medtronic Inc. recalls Medtronic CareLink iPro Therapy Management Software, MMT-7340 The CareLink iPro Therapy Management Software (model,
Medtronic recalls CareLink iPro Therapy Management Software (MMT-7340) due to incorrect glucose reports generated between Sept 23-27, 2017 using the new Uploader feature. Affected healthcare professionals should verify reports from that period.
MedtronicOct 10, 2017 - Lower riskMedical device
Medline Industries Inc recalls MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER, 21.3 in (54 cm) FOR ENDOTRACHEAL TUBE, 12 Fr, REF DYNCSDS12, 1 Each,
Medline recalls sterile double swivel suction catheters that were distributed before sterilization. This could lead to infection if used without proper sterilization. Affected products have specific model and lot numbers.
MedlineOct 10, 2017 - Use cautionMedical device
Crimson Trace Corporation recalls Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used for
Crimson Trace recalls laser sights with Model 25-0657 diode that exceed 5 mW power output. This may cause eye injury. Affected users should contact for remedy.
Crimson TraceOct 10, 2017 - Lower riskMedical device
Karl Storz Endoscopy recalls STORZ High Flow Insufflation Tubing (with filter), Catalog #20400161S/10 (outer box label), ENDOFLATOR 26-430520-1 also
Karl Storz Endoscopy recalls STORZ High Flow Insufflation Tubing (with filter) due to mislabeled pouches inside cardboard boxes. Affected units have incorrect catalog numbers and may be confused with different products.
Karl Storz EndoscopyOct 10, 2017 - Lower riskMedical device
ORTHO SOLUTIONS, LTD. recalls SYSTEM 26. Part Numbers: OS900035-NS; OS900036-NS; OS900037-NS; OS900038-NS; OS900040-NS; OS900041-NS; OS900042-NS;
Ortho Solutions recalls System 26 Forefoot and Midfoot Implants and Instruments trays due to corrosion residue inside the cannulated devices. Affected units include specific part numbers and lot numbers sold in the US market.
Ortho SolutionsOct 10, 2017 - UnratedDrug
Banner Pharmacy Services, LLC recalls Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy
Banner Health recalls hydromorphone syringes with lack of sterility assurance. Affected lots expire by 2018. Consumers should contact pharmacy for details.
Banner HealthOct 10, 2017
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